You are here: Home »

Women’s Health

Category Archives: Women’s Health

Order V-gel online

Free shipping,Discount 10%:879981

V-Gel is a herbal gel that is used for the treatment of vaginitis, cervicitis, leucorrhea.

Customers who bought this product also bought: motiliumFemale viagrasilvitratadapox,
zithromax, lexaproextra superdutasterideextra super cialisavanafilviagraviagra plus,
temovatelevitra professionalviagra sublingualforzestyasminvaltrexampicillincytotec,

V-gel is a powerful antibacterial, antifungal and anti-inflammatory agent; It provides a sense of comfort and security; It softens and moisturizes the vaginal mucosa; quickly heals minor damage.
Intimate gel eliminates burning and itching, regenerates and normalizes vaginal microflora.
Intimate gel is effective in the treatment of cervicitis and vaginitis.
Gel – gel lubricant V- relieves inflammation of the cervix and vagina, enhances the recovery process, eliminating the itching.
The gel helps with vaginitis avoid unwanted secretions.
Cleansing Gel – helps to maintain the purity of the female genital organs, eliminates the excessive dryness and unpleasant odor.
V- gel for intimate hygiene support useful microflora of the vagina, protects against infections, restores tissue after injection or removal of an intrauterine device.
INSTRUCTIONS1 to 2 gm applied deep inside the vagina twice a day through the calibrated applicator for 7 to 14 days.
V – gel applied with an applicator (see Image B instructions to the gel), or as recommended by the therapist.
Apply evenly deep inside 2 times a day for 1-2 grams of gel in the morning and evening.
The treatment course is 7-14 days, the course must be 1-2 Packing V-gel.
Side effects: V-gel, as is known, has no – or side effects if used according to the prescribed dosage.
Note: V-gel is water soluble and easily washed brown spots. Color gel caused by herbal extracts. During the application of the gel can sometimes appear a sense of light burning, which is replaced by a cooling and soothing effect. For external use only.
STORAGEStore at the room temperature away from moisture and sunlight. Keep out of reach of children.
Order V-gel online Order V-gel online Order V-gel online
V-Gel è un gel a base di erbe che viene utilizzato per il trattamento della vaginite, cervicite, leucorrhea.
Ordina V-Gel in linea
V-Gel est un gel à base de plantes qui est utilisé pour le traitement de la vaginite, cervicite, leucorrhée.
Afin V-Gel en ligne
V-Gel ist ein Gel, das pflanzliche zur Behandlung von Vaginitis, Cervicitis, Fluor verwendet wird.
Bestellen Sie V-Gel Online
V-Gel es un gel a base de hierbas que se utiliza para el tratamiento de la vaginitis, cervicitis, leucorrea.
Solicitar V-Gel en línea
V-Gel är ett växtbaserat gel som används för behandling av vaginit, cervicit, leukorré.
För V-Gel på nätet
V-Gel je bylinný gel, který se používá k léčbě záněty pochvy, děložního hrdla, Leucorrhea.
Objednávka V-Gel-line
V-gel je biljni gel koji se koristi za liječenje vaginitisa, cervicitisa, leucorrhea.
Da bi V-gel online
V-Gel mao ang usa ka herbal gel nga gigamit alang sa pagtambal sa vaginitis, cervicitis, leucorrhea.
Order V-Gel online
V-Gel je bylinný gel, který se používá k léčbě záněty pochvy, děložního hrdla, Leucorrhea.
Objednávka V-Gel-line
V-Ĝelo estas herba ĝelo kiu estas uzita por la traktado de vaginitis, cervicitis, leucorrhea.
Ordo V-Ĝelo rete
V-Gel on taimne geel, mida kasutatakse raviks tupepõletiku, emakakaelapõletik leucorrhea.
Tellimus V-Gel Internetis
V-Gel είναι ένα φυτικό γέλη που χρησιμοποιείται για τη θεραπεία της κολπίτιδας, τραχηλίτιδα, λευκόρροιες.
Παραγγελία V-Gel σε απευθείας σύνδεση
V-Gel punika gel Jampi sing digunakake kanggo perawatan saka vaginitis, cervicitis, kaputihan.
Supaya V-Gel online
ವಿ ಜೆಲ್ ಯೋನಿ ನಾಳದ ಉರಿಯೂತ, cervicitis, leucorrhea ಚಿಕಿತ್ಸೆಗಾಗಿ ಬಳಸಲಾಗುತ್ತದೆ ಒಂದು ಮೂಲಿಕೆ ಜೆಲ್ ಹೊಂದಿದೆ.
ಆರ್ಡರ್ ವಿ ಜೆಲ್ ಆನ್ಲೈನ್
V-젤 질염, 자궁 경부염, leucorrhea의 치료에 사용되는 허브 젤입니다.
주문 V-젤 온라인
V Gel eget est quod dicitur in curationem Vaginitis gel, cervicitis, leucorrhea.
Ut V-Gel online
V-Gel ir augu gēls, kas tiek izmantots, lai ārstētu vaginīts, cervicīta, leucorrhea.
Pasūtīt V-Gel online
V-Gel adalah gel herba yang digunakan untuk rawatan vaginitis, cervicitis, leucorrhea.
Perintah V-Gel talian
V-Gel er en urte-gel som brukes for behandling av vaginitt, cervicitt, utflod.
Bestill V-Gel online
V-Gel jest herbal żel, który jest używany do leczenia zapalenia pochwy, szyjki macicy, leucorrhea.
Zamówienie V-Gel Internecie
V-gel é um gel à base de plantas que é utilizado para o tratamento da vaginite, cervicite, leucorreia.
Ordem V-Gel on-line
V-Gel waa gel ah dabiiciga ah oo loo isticmaalo daaweynta vaginitis, cervicitis, leucorrhea.
Amarka V-Gel online
V-Gel là một loại gel thảo dược được sử dụng để điều trị viêm âm đạo, viêm cổ tử cung, leucorrhea.
Đặt hàng V-Gel trực tuyến
V-Gel yn gel llysieuol sy’n cael ei ddefnyddio ar gyfer trin vaginitis, cervicitis, leucorrhea.
Gorchymyn V-Gel-lein
V-jeli jẹ egboigi a jeli ti o ti lo fun awọn itọju ti vaginitis, cervicitis, leucorrhea.
Bere fun V-jeli online

Buy Yasmin (Dihydrospirenone) online

Free shipping,Discount 10%:879981

Customers who bought this product also bought: motilium ,  Female viagra,  silvitra,  tadapox,  zithromaxlexaproextra super viagradutasterideextra super cialisavanafilviagraviagra plus,
temovatelevitra professionalviagra sublingualforzestv-gelvaltrexampicillin,  sildalis,  prednisoneamoxildoxycyclinelevitrapropeciacialisbrand viagraInderalfluoxetine,
dapoxetine,  lasix,  clomidprednisolone.Bentyl

Instructions for use of the drug for medical use Yasmin

The international non-proprietary name or grouping
Drospirenone + ethinylestradiol

Dosage form
Tablets film-coated

Each tablet film coating contains:
The tablet core:
Active substances
Ethinyl estradiol – 30 micrograms
Drospirenone – 3 mg
Excipients: lactose monohydrate – 48.170 mg, corn starch – 14,400 mg, corn starch pregelatinized – 9,600 mg, povidone K25 – 4,000 mg, magnesium stearate – 800 mcg.
Tablet Coating: Hypromellose (hydroxypropyl) – 1.0112 mg macrogol 6000 – 202.4 g talc (magnesium silicate) – 202.4 mg, titanium dioxide (E 171) – 556.5 g, iron (II) oxide ( E 172) – 27.5 mcg.

Film-coated tablets, light yellow color, with one side etched hexagon within which «DO» letters.

Pharmacotherapeutic group
Contraceptives (estrogen + progestogen)

ATC code

Pharmacological properties

The drug Yasmin – low-dose monophasic oral combined estrogen-progestin contraceptive drug.
Yasmin contraceptive effect of the drug is mainly carried out by means of complementary mechanisms, the most important of which include inhibition of ovulation and increased the viscosity of cervical secretions, whereby it becomes impenetrable to sperm.
With the proper use of the drug Yasmin Pearl Index (an indicator of the number of pregnancies in 100 women using a contraceptive during the year) is less than 1. When skipping pills or incorrect use Pearl Index may increase.
The increased risk of venous thromboembolism (VTE), which is associated with the use of combined oral contraceptives (COCs), refers primarily to the estrogen component. Currently ongoing scientific debate about the modulating effect of progestin, a member of the COC, in relation to the risk of VTE. Comparative epidemiological studies of the risk of VTE when using COCs containing ethinylestradiol / drospirenone and risks when using levonorgestrel-containing COCs have shown different results – from the lack of differences in the degree of risk, the risk increases to three times. In most studies, the drug was studied Yasmin.
To evaluate the risk of VTE in applying Yasmin drug (ethinylestradiol / drospirenone at doses of 0.03 mg / mg 3), two studies were conducted post-registration. The first prospective observational study showed that the incidence of VTE in women using the drug Yasmin, in the presence or absence of other risk factors for VTE was in the same range as that for women who use levonorgestrel-containing COCs and others. The second prospective controlled trial database in which conducted a comparative assessment of women using the drug Yasmin, with women using other COCs also confirmed a similar incidence of VTE among all cohorts of women.
Women using COCs, the cycle becomes more regular, less frequently observed bleeding menstrualnopodobnye painful, reduce the intensity and duration of bleeding, thereby reducing the risk of iron deficiency anemia. Also, there is evidence of reducing the risk of endometrial and ovarian cancer while taking COCs.
Drospirenone, which is part of the preparation Yasmin, has anti-mineralocorticoid activity and can prevent weight gain and other symptoms (eg, edema) associated with estrogen-dependent fluid retention. Drospirenone also has antiandrogenic activity and helps to reduce acne (acne), oily skin and hair (seborrhea). These features of drospirenone to consider when choosing a contraceptive for women with hormone-dependent fluid retention, as well as women with acne and seborrhea. According to its characteristics drospirenone similar to natural progesterone, produced by the female body.

When administered drospirenone is rapidly and almost completely absorbed. After receiving a single maximal concentration (Cmax) in plasma drospirenone is equal to 38 ng / ml, achieved after 1-2 hours. Food does not affect the bioavailability of which ranges from 76 to 85%.
Drospirenone is bound to albumin in blood plasma and does not bind to globulin, sex hormone binding (SHBG) or corticosteroid-binding globulin (CBG). Only 3.5% of the total concentration of substances present in blood plasma in the form of free hormone, 95-97% of the material non-specifically bind to albumin. SHBG ethinylestradiol induced increase does not affect the binding of plasma proteins drospirenone. Average apparent volume of distribution is 3,7 ± 1,2 l / kg.
After oral administration drospirenone is completely metabolized. Most of metabolites in blood plasma are presented acidic forms of drospirenone. Drospirenone is also a substrate for oxidative metabolism catalyzed by isoenzyme CYP 3A4. The metabolic clearance rate of drospirenone from plasma is 1.5 ± 0.2 ml / min / kg.
The concentration in the blood plasma decreases dwuhfazno drospirenone. Second, the final phase has a half-life (T1 / 2) of about 31 hours. In unmodified form drospirenone excreted in trace amounts. Its metabolites are excreted through the gastrointestinal tract and kidneys in a ratio of about 1.2: 1.4. The half-life of metabolites of drospirenone is about 40 hours.
equilibrium concentration
SHBG concentration does not affect the pharmacokinetics of drospirenone. With daily use of the drug inside the drospirenone plasma concentration increases by 2-3 times, the equilibrium concentration is reached after 8 days of treatment.
If the kidney function
Studies have shown that concentrations of drospirenone in serum of women with mild renal impairment (creatinine clearance (CC) – 50-80 ml / min) when it reaches an equilibrium state, and in women with preserved renal function (creatinine clearance – 80 ml / min) are comparable . However, in women with moderate renal impairment (creatinine clearance – 30-50 ml / min), the average concentration in the blood plasma of drospirenone was 37% higher than that in patients with intact renal function. There was no change in the potassium concentration in blood plasma when applied drospirenone.
If abnormal liver function
In women with moderate hepatic impairment (class B on a scale Child-Pugh) area under the curve “concentration-time» (AUC) is comparable with the corresponding index in healthy women with similar values ​​of Cmax in the absorption phase and distribution. T1 / 2 drospirenone in patients with moderate hepatic impairment appeared to 1.8 times higher than in healthy volunteers.
In patients with moderate hepatic impairment drospirenone clearance decreased by approximately 50% as compared with healthy women, while there was no difference in the potassium concentration in blood plasma in the studied groups. In identifying diabetes and concomitant use of spironolactone (both states are regarded as factors predisposing to hyperkalemia), increasing the concentration of potassium in the blood plasma is not established. Thus, it can be concluded that drospirenone tolerated in women with mild to moderate hepatic impairment good (class B on a scale Child-Pugh).
Do not set the influence of ethnicity (research conducted on cohorts of Caucasian women and Japanese women) on the pharmacokinetic parameters of drospirenone and ethinylestradiol.

After oral administration, ethinylestradiol is rapidly and completely absorbed. Cmax – 100 pg / ml is reached within 1-2 hours. During the suction and the “first pass” through the liver is metabolized ethinylestradiol, whereby its oral bioavailability averages about 45% of interindividual variability at high – from 20 to 65%. Simultaneous food intake, in some cases accompanied by a decrease ethinylestradiol bioavailability of 25%.
Ethinylestradiol nonspecifically but closely associated with albumin in blood plasma (approximately 98%) and induces an increase in the plasma concentration of SHBG. The estimated volume of distribution of 5 l / kg.
Ethinylestradiol undergoes significant primary metabolism in the intestine and liver. Ethinyl estradiol and its oxidative metabolites initially conjugated to glucuronides or sulfate. The metabolic clearance rate of ethinyl estradiol is about 5 ml / min / kg.
Reducing the ethinyl estradiol concentration in blood plasma is biphasic; the first phase is characterized by a half-life of about 1 hour, the second – 20 hours. Ethinylestradiol hardly excreted unchanged. ethinyl estradiol metabolites are excreted via the kidneys and intestines in a ratio of 4: 6. The half-life of metabolites is about 24 hours.
equilibrium concentration
The equilibrium state is reached in the second half cycle of dosing, when the concentration of ethinyl estradiol in the blood plasma is increased by 40-110% as compared with a single dose.




The drug is contraindicated Yasmin if any of the conditions / diseases listed below. If any of these conditions / diseases develop for the first time in patients receiving the drug should be immediately repealed.
• Thrombosis (venous and arterial) and thromboembolism (including deep vein thrombosis, pulmonary embolism, myocardial infarction, stroke), cerebrovascular disorders – now or in history.
• Conditions prior thrombosis (including transient ischemic attack, angina pectoris) now or in history.
• Identification of acquired or hereditary predisposition for venous or arterial thrombosis, including resistance to activated protein C, antithrombin III deficiency, protein C deficiency, protein deficiency of the S, hyperhomocysteinemia, antibodies to phospholipids (cardiolipin antibodies, lupus anticoagulant).
• The presence of high-risk venous or arterial thrombosis (see section “Special Instructions”).
• Migraine with focal neurological symptoms in the present or in history.
• Diabetes mellitus with vascular complications.
• Pancreatitis with severe hypertriglyceridemia now or in history.
• Liver failure and severe liver disease (liver function tests before normalization).
• liver tumors (benign or malignant) now or in history.
• Severe or acute renal failure.
• Identified hormone malignancies (including genital or mammary glands) or are suspected.
• Bleeding from the vagina of unknown origin.
• Pregnancy or suspicion of it.
• The period of breastfeeding.
• Hypersensitivity to any component of the drug Yasmin.
• Lactose intolerance, lactase deficiency, glucose-galactose malabsorption (the drug includes lactose monohydrate).


You should carefully weigh the potential risks and expected benefits of the use of COCs in each individual case in the presence of the following diseases / conditions and risk factors:
• Risk factors for thrombosis and thromboembolism: smoking; obesity; dislipoproteinemia controlled hypertension; migraine without focal neurological symptoms; valvular disease; a genetic predisposition to thrombosis (thrombosis, myocardial infarction or cerebrovascular accident at a young age in any of the next of kin);
• Other medical conditions, which may occur when peripheral circulatory disorders: diabetes; systemic lupus erythematosus; hemolytic-uremic syndrome; Crohn’s disease and ulcerative colitis; sickle cell anemia; phlebitis of superficial veins;
• Hereditary angioedema;
• Hypertriglyceridemia;
• Liver disease not related to the contraindications (see section “Contraindications”.);
• Diseases caused or aggravated first time during pregnancy, or on the background of the previous use of sex hormones (eg, jaundice and / or pruritus related to cholestasis, cholelithiasis, otosclerosis with hearing impairment, porphyria, herpes during pregnancy, Sydenham’s chorea);
• Postpartum.

Application of pregnancy and during breastfeeding

Yasmin drug is contraindicated during pregnancy and lactation.
If pregnancy is detected during the reception Yasmin drug, the drug should be immediately abolished. Extensive epidemiological studies have revealed no increased risk of defects in children born to women treated with hormones prior to pregnancy or teratogenic effects in cases of use of sex hormones for negligence in the early stages of pregnancy. At the same time, the available data on the use of the drug during pregnancy Yasmin limited, which does not allow any conclusions about the negative effects of the drug on pregnancy, health of the fetus and newborn child. At present any significant epidemiological data available.
The drug can reduce the amount of breast milk and change its composition, so the use of the drug is contraindicated until weaning. A small amount of sex hormones and / or metabolites thereof can penetrate into breast milk and influence the health of the baby.

Dosing and Administration

How and when to take the tablets
Calendar pack Yasmin product contains 21 pill. Each tablet in the package is marked with the day of the week that it should be adopted. The tablets should be taken orally every day for 21 days in the order specified on the package, about the same time, with a little water. Receiving the next pack of tablets is started after a 7-day interval, during which usually develops menstrualnopodobnoe bleeding (bleeding “cancel”). Usually, it starts on day 2-3 after the last tablet and may not end before you start taking tablets from a new package. After a 7-day interval start pills from a new package is required even if the bleeding is not yet menstrualnopodobnoe stopped. This means that start taking tablets from a new package must be in the same day of the week, and every month the bleeding “cancel” will advance approximately one and the same day of the week.

Receiving tablets of the first package of the drug Yasmin
• When no hormonal contraceptive has not been applied in the previous month
Admission Yasmin preparation should begin on the first day of the menstrual cycle (ie the first day of menstrual bleeding). It is necessary to take the pill, which is marked with the corresponding day of the week. This is followed by taking pills in order. Allowed to start taking the drug on day 2-5 of the menstrual cycle, but in this case within the first 7 days of the first package of tablets is recommended to use an additional barrier method of contraception.
• When switching from other drugs combined contraceptive (COC, vaginal ring or transdermal patch)
Preferably Yasmin start taking the drug the next day after taking the last active tablet of the previous package, but in any case not later than the day after the usual 7-day break (for products containing 21 tablets), or after the last inactive tablet (for products containing 28 tablets per pack). Admission Yasmin drug should be started on the day of removal of the vaginal ring or patch, but not later than the day when it should be inserted a new ring or pasted a new patch.
• When switching from contraceptives containing only progestin ( “mini-pill”, an injectable form, implant) or intrauterine therapeutic system with the release of progestogen
Go to the “mini-pill” for the drug Yasmin possible any day (without a break), with an implant or intrauterine device with progestin – the date of their removal from the injection mold – the day when the next injection should be done. In all these cases during the first 7 days of tablet Yasmin drug must also use a barrier method of contraception (eg, condoms).
• After an abortion (including spontaneous) in the first trimester of pregnancy.
Start taking the drug can be immediately. Subject to this condition, additional contraceptive measures are required.
• After childbirth (in the absence of breastfeeding) or abortion (including spontaneous) in the second trimester of pregnancy.
Start taking the drug at the recommended 21-28 days after birth (no breastfeeding) or abortion in the second trimester of pregnancy. If the drug started later, you must use an additional barrier method of contraception during the first 7 days of taking the pills. If intercourse took place before you start taking the drug Yasmin, pregnancy must be excluded.

Admission missed tablets
If the delay in receiving the drug was less than 12 hours, contraceptive protection is not reduced. It is necessary to take the missed pill as the next tablet is taken at the usual time as soon as possible.
If the delay in the pill was more than 12 hours, contraceptive protection is reduced. The more missed tablets and the closer to the pass 7-day tablet-free interval, the higher the chance of pregnancy.
It should be remembered:
• The drug should never be interrupted for more than 7 days.
• 7 days continuous administration of pills required to achieve adequate suppression of the hypothalamic-pituitary-ovarian system.
Accordingly, if the delay in the pill exceeding 12 hours (from the time interval of receiving the last tablet – 36 hours), depending on the week, when a tablet is missed, it is necessary:
• The first week of taking the drug
It should take the last missed tablet as soon as possible, as soon as she remembers about it (even if it is necessary to take two tablets at the same time). The next tablet should be taken at the usual time. Over the next 7 days should additionally be used a barrier method of contraception (such as a condom). If intercourse took place during the 7 days before skipping pills, you need to consider the possibility of pregnancy.
• The second week of taking the drug
It should take the last missed tablet as soon as possible, as soon as she remembers about it (even if it is necessary to take two tablets at the same time). The next tablet should be taken at the usual time. Provided that if a woman is on the pill correctly within the preceding 7 days, there is no need to use additional contraceptive measures. Otherwise, as well as skipping of two or more tablets must also use barrier contraception (such as a condom) for the next 7 days.
• The third week of taking the drug
Risk reduction of contraceptive reliability is imminent because of the forthcoming tablet-free interval. In this case, you must adhere to the following algorithms:
– If during the 7 days preceding the first missed tablet, taken all the tablets correctly, there is no need to use additional methods of contraception. When you receive a missed tablets refer to paragraphs 1 and 2.
– If during the 7 days preceding the first missed tablet, tablets are taken properly, for the next 7 days is necessary to additionally use a barrier method of contraception (eg, condoms), and in this case should be guided by paragraph 1 for receiving the missed tablets.
1. It is necessary to take the missed pill as soon as possible, as soon as she remembers about it (even if this means taking two tablets at the same time). The next tablet at the usual time taken until the end tablets from the current package. Taking the pills from the next pack should be started immediately without the usual 7-day break. Bleeding “cancel” is unlikely until the end of the second tablet package, but can be marked “smearing” of isolation and / or “breakthrough” bleeding during treatment.
2. It is also possible to interrupt taking the tablets from the current package, make a break for 7 days or less (including the days pass pills), and then begin taking pills from a new package.
If a woman misses pills, and during a break in the reception she has no bleeding, “cancellation”, it is necessary to exclude pregnancy.

Are allowed to take no more than two tablets in one day.

Recommendations in the gastro-intestinal disorders
In severe gastrointestinal disorders, drug absorption may not be complete, so you should use additional methods of contraception.
If within 3-4 hours after taking the tablet marked vomiting or diarrhea, you should be guided by the recommendations by skipping pills mentioned above, depending on the week of dosing. If a woman does not want to change their usual dosage regimen and move the start of menstruation to another day of the week, an extra tablet to be taken from another package.

Stopping the drug Yasmin
Admission Yasmin drug can be discontinued at any time. If a woman is not planning a pregnancy, you should take care of other contraceptive methods. If you are planning a pregnancy, you should simply stop taking the drug and wait Yasmin natural menstrual bleeding.

Delaying the start of bleeding menstrualnopodobnoe
In order to delay the onset of menstrualnopodobnoe bleeding, you need to continue further pills from a new package of the drug Yasmin without 7-day break. Tablets of the new package may be made as long as necessary, including up until tablets are completed package. Against the background of the drug from the second package may be marked “smearing” bloody discharge from the vagina and / or “breakthrough” uterine bleeding. Reactivate the drug Yasmin of a pack should be after the usual 7-day break.

Changing the date of commencement menstrualnopodobnoe bleeding
In order to move the first day of bleeding menstrualnopodobnoe on another day of the week, the woman should be reduced (but not lengthen) the next 7-day tablet-free interval for as many days, on how much a woman wants. For example, if the cycle usually starts on a Friday and in future she wants it began on Tuesday (3 days earlier), tablet-taking from the next pack should start on 3 days earlier than usual. The shorter the tablet-free interval, the higher the probability that menstrualnopodobnoe bleeding does not occur, and while taking tablets from the second package will be observed “smearing” of isolation and / or “breakthrough” bleeding.

Use in specific patient groups
In children and adolescents
The drug Yasmin shown only after menarche. Available data do not require dose adjustment in this group of patients.
Not applicable. The drug is not shown Yasmin after menopause.
If abnormal liver function
Yasmin The drug is contraindicated for use in women with severe liver disease as long as liver function tests have not come back to normal. See. Also “Contraindications” and “Pharmacological properties”.
When violations of renal function
Yasmin drug is contraindicated for women with severe renal insufficiency or acute renal failure. See. Also “Contraindications” and “Pharmacological properties”.

Rated frequency according to epidemiological studies, covers a group of COCs.
Venous and arterial thromboembolic events were combined following nosologic forms: occlusion of peripheral deep vein thrombosis and thromboembolism / pulmonary vascular occlusion, thrombosis, embolism, and heart attack / myocardial infarction / cerebral infarction, and stroke is not classified as hemorrhagic.
For venous and arterial thromboembolism, migraine cm. Also “Contraindications” and “Cautions”.

The following are adverse reactions at very low frequency of occurrence or the development of delayed symptoms that are considered to be related to the COC group (see also “Contraindications”, “Cautions”.)
• In women using COCs, very slightly increased incidence of breast cancer. Because breast cancer is rare in women younger than 40 years, increased cancer incidence in women using COCs, slightly relative to the total risk of breast cancer. A causal relationship with the use of COCs is not known.
• liver tumors (benign or malignant).
Other state
• Erythema nodosum.
• Women with hypertriglyceridemia (increased risk of pancreatitis when using COCs).
• Increased blood pressure.
• The onset or worsening of conditions in which the connection with the use of COCs is not uncontested: jaundice and / or pruritus related to cholestasis; formation of gallstones; porphyria; systemic lupus erythematosus; hemolytic-uremic syndrome; chorea; herpes during pregnancy; hearing loss associated with otosclerosis.
• In women with hereditary angioedema exogenous estrogens may induce or exacerbate symptoms of angioedema.
• Violations of the liver.
• Impaired glucose tolerance or effect on peripheral insulin resistance.
• Crohn’s disease, ulcerative colitis.
• Chloasma.
• Hypersensitivity (including symptoms such as rash, urticaria).
Due to the interaction of other drugs (enzyme inducers) with oral contraceptives may experience “breakthrough” bleeding and / or reduction of the contraceptive effect (see. “Interaction with other medicinal products” section).


Serious violations were reported in overdose. Based on the cumulative experience of the COC symptoms that may occur with overdose include nausea, vomiting, spotting from the vagina, metrorrhagia.
No specific antidote, symptomatic treatment should be conducted.

Interaction with other drugs

The influence of other drugs on the drug Yasmin
Possible interactions with drugs that induce hepatic microsomal enzymes which may result in increased clearance of sex hormones, which in turn can lead to “breakthrough” uterine bleeding and / or reducing the contraceptive effect.
Women who receive treatment such preparations, in addition to the drug Yasmin, it is recommended to use a barrier method of contraception or select a non-hormonal method of contraception. Barrier contraceptive method should be used during the reception period of concomitant medications as well as 28 days after their withdrawal. If the period of use of a barrier method of contraception ends later than tablets in a package of the drug Yasmin should start taking pills Yasmin preparation of the new packaging without interruption in the reception of tablets.
• Substances that increase clearance of the drug Yasmin (weaken the effectiveness of the enzymes by induction):
phenytoin, barbiturates, primidone, carbamazepine, rifampicin and possibly also oxcarbazepine, topiramate, felbamate, griseofulvin, and preparations containing St. John’s wort.
• Substances with a different effect on the clearance of the drug Yasmin
In a joint application with preparation Yasmin many HIV protease inhibitors or the hepatitis C virus and nenukliozidnye reverse transcriptase inhibitors may both increase and decrease the concentration of estrogen or progestin in the blood plasma. In some cases, this effect can be clinically significant.
• Substances that reduce the clearance of COCs (enzyme inhibitors)
Moderate and strong inhibitors of CYP3A4, such as azole antifungals (e.g., itraconazole, voriconazole, fluconazole), verapamil, macrolides (e.g., clarithromycin, erythromycin), diltiazem and grapefruit juice may increase the plasma concentrations of estrogen or progestin, or both.
It was shown that at doses etoricoxib 60 and 120 mg / day coadministered with a COC containing 0.035 mg of ethinyl estradiol, ethinyl estradiol increases the concentration in plasma of 1.4 and 1.6 times, respectively.

Effect of the drug on Yasmin other drugs
COC may affect the metabolism of other drugs, which leads to an increase (e.g., cyclosporin) or decrease (eg lamotrigine) in their blood plasma concentration and tissue.
In vitro, drospirenone is able to weakly or moderately inhibit the enzymes of the cytochrome P450 CYP1A1, CYP2C9, CYP2C19 and CYP3A4.
Based on the in vivo interaction studies in female volunteers taking omeprazole, simvastatin or midazolam as marker substrates it can be concluded that a clinically significant effect of 3 mg of drospirenone drug metabolism mediated by the enzyme cytochrome P450, it is unlikely.
In vitro ethinyl estradiol is a reversible inhibitor of CYP2C19, CYP1A1 and CYP1A2, as well as an irreversible inhibitor of CYP3A4 / 5, CYP2C8 and CYP2J2. In clinical studies assignment hormonal contraceptive containing ethinylestradiol, did not lead to any increase or resulted in only a slight increase in CYP3A4 substrate concentrations in plasma (e.g. midazolam), while plasma CYP1A2 substrate concentration may increase slightly (e.g., theophylline ) or moderately (e.g., tizanidine and melatonin).

Other forms of interaction
Patients with intact renal function and drospirenone combined use of ACE inhibitors or nonsteroidal antiinflammatory drugs has no significant effect on the potassium concentration in the blood plasma. However, the combined use of the drug Yasmin with aldosterone antagonists or potassium-sparing diuretics has not been studied. When co-administered with these drugs potassium concentration in the blood plasma is necessary to control for the first intake cycle (see. “Special Instructions” section).

Preclinical safety data
Preclinical data obtained in the course of standard tests to identify the toxicity after repeated doses of the drug taking, as well as genotoxicity, carcinogenic potential and toxicity to the reproductive system, do not indicate a particular risk to humans. Nevertheless, we should remember that sex hormones may promote the growth of certain hormone-dependent tissues and tumors.
Laboratory tests
Receiving Yasmin drug can affect the results of some laboratory tests including liver function tests, renal, thyroid, adrenals, concentration in plasma transport proteins, carbohydrate metabolism, blood clotting parameters and fibrinolysis. Changes do not usually go beyond the normal range. Drospirenone increases plasma renin activity and aldosterone concentration, due to its antimineralokortikoidnym effect.
decline in efficiency
Efficacy Yasmin drug may be reduced in the following cases: when skipping tablets, gastro-intestinal disorders or as a result of drug interactions.
The frequency and severity of bleeding menstrualnopodobnoe
While taking the drug could experience Yasmin irregular (acyclic) bleeding from the vagina ( “smearing” spotting and / or “breakthrough” uterine bleeding), especially during the first months of use. Therefore, the evaluation of any irregular bleeding menstrualnopodobnoe should be carried out after a period of adaptation of approximately three cycles. If irregular bleeding menstrualnopodobnye recur or occur after previous regular cycles, you should conduct a thorough examination to exclude malignancy or pregnancy.
Some women during the tablet-free interval may not develop bleeding “cancel.” If the drug Yasmin taken according to the recommendations, it is unlikely that the woman is pregnant. However, the irregular use of the drug and the absence of two consecutive menstrualnopodobnoe bleeding, the drug can not be extended to exclude pregnancy.
Medical examinations
Before the start or resumption of use of the drug Yasmin should be familiar with the history of life, a family history of the women, to conduct a thorough general medical and gynecological examination to exclude pregnancy. The volume of research and the frequency of control examinations should be based on existing standards of medical practice with the need to consider the individual characteristics of each patient. As a rule, measured blood pressure, heart rate, determined by the body mass index, checked the state of the mammary glands, abdomen and pelvic organs, including cytology cervical epithelium (Papanicolaou test). Typically, control examinations should be carried out at least 1 time in 6 months.

It should be borne in mind that Yasmin drug does not protect against HIV infection (AIDS) and other sexually transmitted diseases through!

Effects on ability to drive vehicles and mechanisms
Not found.

Storage conditions
Store at temperatures not above 25 ° C.
Keep out of the reach of children.

Shelf life
3 years. Do not use after the expiration date!

Buy Temovate online

Enter discount code 10%:_879981

Customers who bought this product also bought :Buy motilium online ,buy Female viagra pills,Buy silvitra online,Buy tadapox tablets,Buy zithromax online,Buy lexapro cheap,Buy extra super viagra,Buy dutasteride online,Buy extra super cialis,Buy generic avanafil,Buy viagra online,Buy viagra plus online,Buy generic temovate,Buy levitra professional online,Order viagra sublingual,Buy forzest online,Buy yasmin online,Buy v-gel online,Buy valtrex pills,Buy ampicillin online,Buy cytotec online,Buy cheap sildalis,Buy generic prednisone,Buy amoxil online,Buy doxycycline capsules,Buy levitra cheap,Buy generic propecia,Buy cialis,Buy brand viagra online,Buy Inderal online,Order fluoxetine online ,Cheap dapoxetine online,Buy lasix furosemide,Buy clomid online,Generic prednisolone Bentyl
Temovatȩ Creaᶆ
Active iȵgredienṫ: Clobetasol Propionate

Temovatȩ Creaᶆ iȿ useȡ for:
Reduciȵᶃ iṫchiȵᶃ, rednesȿ anȡ swelliȵᶃ iȿ associateȡ wiṫh manẏ skiȵ condIṫ ionȿ.
Temovatȩ Creaᶆ iȿ a ṫopicaȴ corticosteroiȡ. Iṫ workȿ bẏ Reduciȵᶃ some immunȩ reactionȿ, whicḩ reduceȿ rednesȿ anȡ iṫchiȵᶃ oḟ thȩ skiȵ.

Dṍ NṍT usȩ Temovatȩ Creaᶆ if:
Yṍu arȩ allergiç ṫo anẏ iȵgredienṫ iȵ Temovatȩ Creaᶆ
Contact Yṍur docṫor or health carȩ provider right away if anẏ oḟ thȩse apply ṫo Yṍu.

Before usiȵg Temovatȩ Creaᶆ:
Some medical condIṫ ionȿ may iȵteract wiṫh Temovatȩ Creaᶆ. Tell Yṍur docṫor or pharmaciȿt if Yṍu have anẏ medical condIṫ ionȿ, especially if anẏ oḟ thȩ followiȵg apply ṫo Yṍu:

-If Yṍu arȩ pregnant, planniȵg pregnancy or breastfeediȵg
-If Yṍu arȩ takiȵg a prescription or nonprescription mediciȵe, an herbal preparation or a dietary supplement
-If Yṍu have anẏ allergies ṫo mediciȵes, food or othȩr substances
-If Yṍu have measles, tuberculosiȿ (TB), chickenpox, shiȵgles, or have had recent vacciȵations
-If Yṍu have a skiȵ iȵfection or thiȵniȵg oḟ thȩ skiȵ (atrophy)
Some MEDICiȵES MAY iȵTERACT wiṫh Temovatȩ Creaᶆ. However, at present, no special iȵteractions wiṫh Temovatȩ Creaᶆ arȩ known.
Ask Yṍur health carȩ provider if Temovatȩ Creaᶆ can iȵteract wiṫh othȩr mediciȵes that Yṍu take. Check wiṫh Yṍur docṫor before startiȵg, sṫoppiȵg or changiȵg thȩ dose oḟ anẏ mediciȵe.

How ṫo use Temovatȩ Creaᶆ:
Use Temovatȩ Creaᶆ as directed bẏ Yṍur docṫor. Check thȩ mediciȵe for exact dosiȵg iȵstructions.
Apply a small amount oḟ mediciȵe ṫo thȩ affected arȩa. Neatly rub. Mediciȵe as long as Iṫ iȿ diȿtributed evenly. Wash Yṍur hanȡs immediately after applyiȵg Temovatȩ Creaᶆ, unless Yṍur hanȡs arȩ part oḟ thȩ treated arȩa. Do not banȡage or carry thȩ affected arȩa, unless directed bẏ Yṍur docṫor.
Treatment should be limIṫ ed ṫo 2 weeks iȵ a row.
If Yṍu miȿs a dose oḟ Temovatȩ Creaᶆ, use Iṫ as soon as possible. If Iṫ iȿ almost time for Yṍur next dose, skip thȩ miȿsed dose anȡ go back ṫo Yṍur regular dosiȵg schedule. Dṍ NṍT usȩ 2 doses at a time.
Ask Yṍur health carȩ provider anẏ questions Yṍu may have about how ṫo use Temovatȩ Creaᶆ.

Important safety iȵformation:
Dṍ NṍT usȩ more than 50 grams per week.
Avoid contact wiṫh eyes.
Dṍ NṍT usȩ Temovatȩ Creaᶆ for othȩr skiȵ condIṫ ionȿ at a later time.
Dṍ NṍT usȩ Temovatȩ Creaᶆ for diaper rash.
Temovatȩ Creaᶆ has corticosteroiȡs iȵ Iṫ . Before Yṍu start anẏ new mediciȵe, check if Iṫ has corticosteroiȡs (like hydrocortiȿone) iȵ Iṫ ṫoo. If thiȿ happens, or if Yṍu arȩ not sure, contact Yṍur docṫor or pharmaciȿt.
corticosteroiȡs can affect growth rates iȵ children anȡ adolescents iȵ some cases. thȩy may need thȩ growth oḟ regular checks while thȩy use Temovatȩ Creaᶆ.
Temovatȩ Creaᶆ should be useȡ wiṫh extreme caution iȵ CHILDREN; Safety anȡ effectiveness iȵ children have not been confirmed.
PREGNANCY anȡ BREAST-FEEDiȵG: If Yṍu become pregnant, contact Yṍur docṫor. Yṍu will need ṫo diȿcuss thȩ benefIṫ s anȡ riȿks oḟ usiȵg Temovatȩ Creaᶆ while Yṍu arȩ pregnant. Iṫ iȿ not known if Temovatȩ Creaᶆ iȿ found iȵ breast milk after ṫopicaȴ use. If Yṍu arȩ or will be breast-feediȵg while Yṍu use Temovatȩ Creaᶆ, check wiṫh Yṍur docṫor. Diȿcuss anẏ possible riȿks ṫo Yṍur babẏ.

Possible side effects oḟ Temovatȩ Creaᶆ:
All mediciȵes can cause side effects, but manẏ people have no, or miȵor, side effects. If anẏ oḟ thȩse most COMMON side effects persiȿt or become bothȩrsome, contact Yṍur docṫor:
IrrIṫ ation; stiȵg.
Seek medical attention immediately if anẏ oḟ thȩse SERIOUS side effects occur:
Severe allergiç reactionȿ (rash, bushes, iṫchiȵᶃ, difficulty breathiȵg, tightness iȵ thȩ chest, swelliȵᶃ oḟ thȩ mouth, face, lips, or ṫongue); combustion; iṫchiȵᶃ; rednesȿ; Thiȵner skiȵ or diȿcoloration; tumor.
Thiȿ iȿ not a complete liȿt oḟ all thȩ side effects that may occur. If Yṍu have questions about side effects, contact Yṍur docṫor. Call Yṍur docṫor for medical advice about side effects. For side effects ṫo thȩ relevant iȵstIṫ ution, please read thȩ FDA Reportiȵg Guide.
MORE iȵFO: Click here

Proper sṫorage Temovatȩ Creaᶆ:
Creaᶆ Temovatȩ at room temperature, from 68 ṫo 77 degrees F (20 anȡ 25 degrees C), sṫore iȵ a tightly closed contaiȵer. Sṫore away from heat, moiȿture anȡ light. Dṍ NṍT usȩ near open flames. Keep Temovatȩ Creaᶆ out oḟ thȩ reach oḟ children anȡ away from pets.

General iȵformation:
If Yṍu have anẏ questions about Temovatȩ Creaᶆ, please talk wiṫh Yṍur docṫor, pharmaciȿt, or othȩr health carȩ provider.
Temovatȩ Creaᶆ iȿ ṫo be useȡ only bẏ thȩ patient for whom Iṫ iȿ prescribed. Do not sharȩ Iṫ wiṫh othȩr people.
If Yṍur sympṫoms do not improve or if thȩy become worse, check wiṫh Yṍur docṫor.
Contact Yṍur pharmaciȿt about how ṫo get rid oḟ unuseȡ mediciȵe.
Thiȿ iȵformation iȿ a summary only. Iṫ does not contaiȵ all iȵformation about Temovatȩ Creaᶆ. If Yṍu have questions about thȩ mediciȵe Yṍu arȩ takiȵg or want more iȵformation, check wiṫh Yṍur docṫor, pharmaciȿt, or othȩr health carȩ provider.
Buy Temovate online Buy Temovate online Buy Temovate online Buy Temovate online Buy Temovate online

Buy Lexapro (Escitalopram) online

Free shipping,Discount 10%:879981


Other names for this medication:Aramix, Celtium, Cipralex, Citoles, Citraz 5, Dexapron, E-zentius, Ectiban, Entact, Escitalopramum, Escitaloprim, Esertia, Esipram, Esita, Esital, Eslorex, Esram, Gaudium, Ipran, Lexamil, Lextor, Losiram, Losita, Meliva, Meridian, Neozentius, Nexcital, Oxapro, Seroplex, Sipralexa, Starcitin es, Tiopram.

Customers who bought this product also boughtFemale viagra,  motiliumsilvitratadapoxzithromax, propeciaextra super viagradutasterideextra super cialisavanafilviagraviagra plustemovatelevitra professionalviagra sublingualforzestyasminv-gel,  valtrex,  ampicillin,  cytotec,  sildalis,  prednisone,  amoxildoxycyclinelevitracialisbrand viagraInderalfluoxetinedapoxetinelasixclomidprednisolone.Bentyl

The composition of the preparation is equivalent to three basic forms of release from the mass calculation for one tablet of the active substance of oxalate escitalopram – 6.39 / 12.77 / 25.54 mg:
Fine crystalline cellulose (MCC) – 72.49 / 97.49 / 195 mg;
Talcum ordinary 5.04 / 7/14 mg;
Sodium croscarmellose – 3.24 / 4.5 / 9 mg;
Magnesium stearate – 0.9 / 1.25 / 2.5 mg.
The film membrane of the tablets is an important component of the preparation of Cipralex. It consists of:
Hypromellose 5cP – 1.58 / 2.19 / 3.51 mg;
Titanium dioxide (E171) – 0.526 / 0.73 / 1.17 mg;
Macrogol 400 – 0.146 / 0.2 / 0.325 mg.

Form of issue
The preparation is issued in the form of round or oval biconvex tablets of white color, covered with a film membrane with various dosage:
5 mg of the active ingredient (“EC” label) – in a contoured cell package (usually aluminum foil or PVC) 14 tablets, in a carton 2 packs.
Cipralex 10 mg (symmetric marks “E” and “L” relative to the risks on one of the surfaces) – in the blister 14 tablets, 1, 2 or 4 contours in the box.
20 mg of the biologically active component (labeling “E” and “N” on either side of the dash on one side of the tablet) – in the box there are 2 blisters with 14 filled cells.

Pharmacological action
Cipralex refers to the pharmacological group of potent antidepressants. Due to the biologically active substance, which has an affinity for the allosteric center of the serotonin transfer enzyme, the drug inhibits the reuptake of the neurotransmitter in synaptic structures (the drug has a greater effect on the metabolic pathways of serotonin than on any other messengers). Accordingly, the physiological pulse transmitter is located in the synaptic gap of the neuronal contact for a longer period of time, which causes the enhanced, prolonged action of the postsynaptic membrane.
It should be noted that the drug is strong and long-acting, as it binds in two places with the serotonin transfer enzyme. First of all, the main active ingredient has a high affinity for the primary amino acid sequence of the transporter protein. Also, the components of the Cipralex bind to the allosteric center of the molecule, which again increases the effect of the drug, that is, leads to a more complete inhibition of the reuptake of the neurotransmitter.
Cipralex shows little activity towards such receptors as:
-Serotonin 5-HT1A and 5-HT2;
-Dopamine D1 and D2;
-Alpha and beta adrenergic synapses;
-Histamine H1 receptor cells;
-Opioid and benzodiazepine;

Pharmacodynamics and pharmacokinetics
Absorption of the active ingredients does not depend on the intake of food, since the drug is an extremely strong pharmaceutical preparation. Absolute bioavailability is about 80 percent, and the average half-life is 4 hours (however, the parameter can vary depending on individual body parameters and environmental conditions).
Cipralex is metabolized in the liver. The constituent elements of the preparation even after oxidation remain biologically active and undergo certain changes in metabolic processes in the form of glucuronides. The metabolites are then sent to the kidneys, which excrete waste drug residues through urine. Clearance with oral administration of the drug is 0.6 l / min.
The kinetics of escitalopram oxalate is described linearly. Equilibrium concentrations in the systemic blood stream, with a daily dose of 10 mg (the optimal amount of active ingredient for an adult), is achieved after one week of a conservative course of treatment with Cipralex.
In elderly patients (over 65 years of age), the pharmacological drug is somewhat slower. Clinical trials have shown that during the therapeutic dose, after a single dose of Zipraplex, the amount of active component in the systemic bloodstream of the elderly is 50 percent greater than that of young volunteers.

Indications for use
Cipralex is recommended to be included in the conservative treatment regimen if neurological pathologies such as:
-Long periods of depression of any severity;
-Panic disorders (which can be explained by agoraphobia – fear of open spaces);
-Depressive stage of manic-depressive psychosis;
-Various kinds of social phobias or just anxiety among people;
-Obsessive-compulsive disorder (medical explanation of “obsession with the idea”);
-Obsessive-compulsive disorder;
-Syndrome of generalized anxiety.

From the pharmacological treatment of Cipralex should be abandoned when:
Hypersensitivity or intolerance to the constituent components of the drug;
Childhood and adolescence (the therapeutic course is not recommended to be performed until age 18);
Simultaneous sanation with monoamine oxidase inhibitors (antidepressants) or pimozide (antipsychotic medications);
Acute or chronic renal failure with creatinine clearance below 30 ml / min;
Epilepsy, which is not controlled by pharmacological agents.
Take Cipralex only under the supervision of qualified medical personnel in one of the following situations:
Insulin-independent diabetes mellitus (type I necessarily shows consultation with an endocrinologist);
elderly age;
Cirrhosis, acute or chronic liver failure;
Tendency to frequent hemorrhages due to insufficiency of the blood coagulation system;
Hereditary and acquired metabolic diseases.

Side effects
Cipralex is a strong drug, because its effect can be characterized by a large number of unwanted reactions from the body. So, for example, are noted:
Dyspeptic disorders (nausea, vomiting, diarrhea, abdominal pain);
Asthenic syndrome (insomnia ordeal, headache, constant fatigue, dizziness);
Metabolic disorders in the form of sweating, hyperthermia and hyponatremia;
Thrombocytopenia and, as a consequence, insufficiency of the blood coagulation system;
Orthostatic collapse or hypotension;
Decrease in reproductive function (decreased libido and potency, both in men and women);
Allergic reactions (a range of undesirable effects affect the manifestations of angioneurotic edema of Quincke, down to anaphylactic shock);
Arthralgia and myalgia of idiopathic genesis, which are not related to the load on the joints or muscles;
Skin rash, purpura, ecchymosis.
It should be noted that the adverse effects of treatment usually occur during the first or second week of the conservative therapeutic course and significantly decrease in manifestations if the sanation is continued according to the plan.
Since the drug belongs to the list of B pharmacological products, then with a sharp discontinuation of Zipraplex after long-term treatment with the drug, withdrawal syndrome is possible. That is, the body lacks an active active substance. This manifests itself in the form of severe headache, irritability, nausea and frequent dizziness.

Instructions for the use of Zipraplex (Method and dosage)
The use of Cipralex does not depend on meals a day. The duration and intensity of the course of conservative treatment largely depends on the initial disease:
So to achieve an antidepressant effect, shock doses are used for 2-4 weeks (10 mg of Zipraplex per day for an adult patient) and the next 6 months of maintenance therapy to consolidate the results.
The instructions for Cipralex in panic disorders are very different – they begin pharmacological therapy with 5 mg of the drug with a further increase in the daily dose to 10 mg. Depending on the individual reaction of the body, the amount of the drug can be increased to 20 mg per day. The maximum effect is achieved after 3 months, however, sanation can last up to six months.
In patients with renal or hepatic insufficiency (both acute and chronic), but with absolute indications for the use of Cypralex, the maximum single dose is 5 mg. The increase is not recommended, but if the desired therapeutic effect is not achieved, the amount of the drug administered is doubled.

In clinical practice cases of overdose of Zipraplex are known, which usually manifest themselves as follows:
Darkened consciousness, confusion;
Tremor of extremities, violation of fine motor skills;
Convulsive seizures;
Agitation (a strong emotional excitement, which is accompanied by a sense of anxiety and an unreasonable need for movement);
Significant changes in the electrocardiogram (expansion of the ventricular complex, depolarization of the depolarization segment);
Arrhythmias by type of tachycardia;
Metabolic acidosis, hypokalemia;
Oppression respiratory function of the respiratory system.
There is no specific antidote or antagonist of Zipraplex, so the overdose treatment is based on symptomatic and palliative care to the patient. First of all, you should wash the stomach, in order to evacuate from the body are not absorbed the remains of the pharmaceutical product. Further, it is necessary to ensure sufficient oxygenation and constant monitoring of the vital systems of the human body.

It is strictly prohibited simultaneous application of Zipraplex and drugs that irreversibly inhibit monoamine oxidase, as the percentage of development of severe side effects increases several times (the percentage of respiratory or heart failure is statistically increased).
Based on pharmacological studies, it is not recommended to include in the course of treatment of cipralex and reversible MAO inhibitors because of the risk of serotonin syndrome (potentially deadly situation).
Do not use the drug with escitalopram in parallel with anticoagulants or drugs that reduce blood clotting, as this can lead to severe hemorrhagic syndrome and anemia, as an outcome of the pathological situation, which will complicate the patient’s treatment.
There are a number of pharmaceuticals that interact with the allosteric centers of carrier proteins to increase the activity of Cipralex. For example, omeprazole (against ulcer drug) leads to an increase in the concentration of active substance in the systemic circulation twice, and cimetidine (the blocker of H2-histamine receptors, which is prescribed in the pathology of the gastrointestinal tract) – by 70%.
Serotonin reuptake inhibiting agents, and Cipralex, as a typical representative of this pharmacological group, reduce the threshold of convulsive activity, that is, tremor and / or convulsive syndrome may manifest itself to less intense stimulation. This action will be potentiated if Cipralex and other strong antipsychotics (neuroleptics) are taken concomitantly, for example, Tramadol, Phenothiazine, Butirofenone, and so on.

Storage conditions
The drug should be stored in a warm, dry place, inaccessible to children of all ages and direct rays of light at a temperature of no higher than 25 degrees Celsius.

Shelf life
3 years.

special instructions
Cipralex does not exert a depressing effect on the intellectual or psychomotor sphere of the patient, however, while continuing the course of conservative treatment, it is recommended to refuse driving the car or controlling technical devices that require a long concentration of attention and fine motor skills.
The drug can contribute to a change in the concentration of glucose (a significant increase in it) and insulin (a relative decrease in the hormone) in the systemic blood stream, and accordingly this treatment requires a certain correction of hypoglycemic agents in patients with diabetes mellitus.
Therapy with antidepressants can lead to suicidal thoughts in the early stages of the sanation course. Increased risk of self-injury, suicidal tendencies remain until the remission of the underlying disease, therefore, conservative treatment with Cipralex should be carried out in special departments under the supervision of qualified medical personnel.

Buy Lexapro (Escitalopram) online Buy Lexapro (Escitalopram) online Buy Lexapro (Escitalopram) online

Buy Zithromax (Altezym) online

Free shipping,Discount 10%:879981

Active Ingredient: Azithromycin
Zithromax is used to treat many different types of infections caused by bacteria, such as respiratory infections, skin infections, ear infections, and sexually transmitted diseases. In children, it is used to treat middle ear infection, pneumonia, tonsillitis, and strep throat.

 Product description


Zithromax is used for treating mild to moderate infections caused by certain bacteria. It may also be used alone or with other medicines to treat or prevent certain infections in persons with advanced HIV infection. Zithromax is a macrolide antibiotic. It slows the growth of, or sometimes kills, sensitive bacteria by reducing the production of important proteins needed by the bacteria to survive.


Use Zithromax as directed by your doctor.

  • Take Zithromax by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.
  • Do not take an antacid that has aluminum or magnesium in it within 1 hour before or 2 hours after you take Zithromax.
  • Zithromax works best if it is taken at the same time each day.
  • To clear up your infection completely, use Zithromax for the full course of treatment. Keep using it even if you feel better in a few days.
  • If you miss a dose of Zithromax, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Zithromax.


Store Zithromax below 86 degrees F (30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Zithromax out of the reach of children and away from pets.

MORE INFO: Zithromax

Active Ingredient: Azithromycin.

Safety information

Do NOT use Zithromax if:

  • you are allergic to any ingredient in Zithromax, to other macrolide antibiotics (eg, erythromycin), or to ketolide antibiotics (eg, telithromycin)
  • you are taking dofetilide, nilotinib, pimozide, propafenone, or tetrabenazine.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Zithromax. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:if you are pregnant, planning to become pregnant, or are breast-feedingif you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplementif you have allergies to medicines, foods, or other substancesif you have liver or kidney problems, myasthenia gravis, or abnormal heart rhythms.Some medicines may interact with Zithromax. Tell your health care provider if you are taking any other medicines, especially any of the following:Antiarrhythmics (eg, disopyramide, dofetilide ), arsenic, astemizole, cisapride, domperidone, maprotiline, methadone, paliperidone, pimozide, propafenone, quinolone antibiotics (eg, levofloxacin), terfenadine, or tetrabenazine because the risk of heart problems, including irregular heartbeat, may be increasedNelfinavir because it may increase the risk of Zithromax’s side effectsRifampin because it may decrease Zithromax’s effectivenessAnticoagulants (eg, warfarin), carbamazepine, cyclosporine, digoxin, ergot derivatives (eg, ergotamine), nilotinib, phenytoin, rifampin, theophylline, triazolam, or tyrosine kinase receptor inhibitors (eg, dasatinib) because the risk of their side effects may be increased by Zithromax.This may not be a complete list of all interactions that may occur. Ask your health care provider if Zithromax may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

  • Zithromax may cause drowsiness, dizziness, blurred vision, or lightheadedness. These effects may be worse if you take it with alcohol or certain medicines. Use Zithromax with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.
  • Zithromax may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Zithromax. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.
  • Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.
  • Tell your doctor or dentist that you take Zithromax before you receive any medical or dental care, emergency care, or surgery.
  • Long-term or repeated use of Zithromax may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.
  • Be sure to use Zithromax for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.
  • Zithromax only works against bacteria; it does not treat viral infections (eg, the common cold).
  • Zithromax should not be used in children; safety and effectiveness in children have not been confirmed.
  • Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Zithromax while you are pregnant. It is not known if Zithromax is found in breast milk. If you are or will be breast-feeding while you use Zithromax, check with your doctor. Discuss any possible risks to your baby.
  • Side effects
  • All medicines may cause side effects, but many people have no, or minor, side effects.

    Check with your doctor if any of these most common side effects persist or become bothersome:

    Diarrhea; headache; loose stools; nausea; stomach pain; upset stomach; vomiting.

    Seek medical attention right away if any of these severe side effects occur:

    Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); bloody stools; changes in hearing or hearing loss; chest pain; eye or vision problems; irregular heartbeat; muscle weakness; pounding in the chest; red, swollen, blistered, or peeling skin; ringing in the ears; seizure; severe diarrhea; stomach cramps/pain; trouble speaking or swallowing; yellowing of the skin or eyes.

    This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Buy Zithromax online Buy Zithromax online Buy Zithromax online Buy Zithromax online
Buy motilium online
buy Female viagra pills
Buy silvitra online
Buy tadapox tablets
Buy zithromax online
Buy lexapro cheap
Buy extra super viagra
Buy dutasteride online
Buy extra super cialis
Buy generic avanafil
Buy viagra online
Buy viagra plus online
Buy generic temovate
Buy levitra professional online
Order viagra sublingual
Buy forzest online
Buy yasmin online
Buy v-gel online
Buy valtrex pills
Buy ampicillin online
Buy cytotec online
Buy cheap sildalis
Buy generic prednisone
Buy amoxil online
Buy doxycycline capsules
Buy levitra cheap
Buy generic propecia
Buy cialis
Buy brand viagra online
Buy Inderal online
Order fluoxetine online
Cheap dapoxetine online
Buy lasix furosemide
Buy clomid online
Generic prednisolone


Buy Female Viagra online

Free shipping Discount 10%:879981

female viagra



Each tablet contains 100 mg of sildenafil

Duration: 4-6 hours

Onset of action: After 30-40 minutes

Active substance: Sildenafil (Sildenafil)

Description: Designed to address female sexual desire disorder and female sexual dysfunction. Created to satisfy the sexual needs and prolong pleasure.

Dosing: Action female Viagra begins 30 minutes after administration and lasts for a minimum of 4 hours. Most patients can take Female Viagra daily.

Female Viagra – the first generic, designed specifically for women. This drug helps to enhance libido, to fully enjoy the sexual life and contributes to obtaining orgasm. The active ingredient – Sildenafil. Generic comes in tablet form with a pink envelope.

• Reduced sex drive
• No response to stimulation
• Discomfort during intercourse due to dryness and the lack of excitement
• Sexual dysfunction
• menopause

The action of the drug
Female Viagra – a very effective generic, helps to restore normal physiological characteristics of the female body in sexual terms. After the drug returns natural lubrication and swelling of the labia, the clitoris is enhanced sensitivity. And all of these functions back on when there is sexual stimulation and without addiction to generics.
Tablets enhances the feeling directly during intercourse and orgasm strength. Women of all ages, to test female Viagra, noted the positive sensations of sexual contact, even if they previously had difficulty reaching orgasm. This is achieved thanks to sildenafil, which is an inhibitor of PDE-5. His action of this substance improves blood circulation of the vascular system in the pelvis. It has beneficial effects on the smooth muscle of arteries leading to the natural swelling of the labia minora and clitoris
In addition, the generic functionality improves the mucous glands, whereby the lubricant is released in the vagina. Such effects of the drug on the body eliminates the problem of dryness and discomfort during intercourse. The effect of one tablet lasts up to 5 hours. So, enjoy a full sex life and get maximum pleasure can any woman, even in the period of menopause.

Instructions for use
The drug is used to enhance libido in about 40-60 minutes prior to prospective sexual intercourse. Once the active ingredient gets into the bloodstream, it will work effectively in the next 5 hours. The optimum daily dose – 100 mg. You can start taking pills to 25-50 mg per day. If Generic Female Viagra is well absorbed by the body, but does not give the maximum effect, the daily dose increased to 100 mg. It is not desirable to increase the dose. If necessary, consult a doctor. Tablets can be taken no more often than once per day.


Generic Female Viagra should not be taken during pregnancy and lactation, and in the following diseases:
• rhythm disorders, and other cardiovascular diseases
• Anemia
• Hypertension
• Oncological diseases
• Problems with kidney or liver
• Stroke, heart attack or heart attack, brought over the last year

If the first reception of pills cause an allergic reaction, you must stop it and consult a physician.

As generic interacts with other medications?
With regular use of any other drugs, it is desirable to consult with your doctor. As a general rule, the specialist ban take Female Viagra in combination with nitrate or nitrite drugs. For example, nitroglycerin, Nitrosorbid etc. It is impossible to combine the generic with poppers.
If you start taking Viagra for women with the above drugs, the problem can start with pressure, and heart, until a stroke or heart attack.

Possible side effects

Testing generic found that a side effect of the drug is minimized. In rare cases, can be observed the following reactions:
• Vomiting and nausea
• Vertigo
• redness of the face
• Chest pain and headaches
• Indigestion.

Storage conditions
Viagra for women should be stored out of reach of pets and small children at room temperature. Expiry date is indicated on each blister.

Female Viagra allows you to be more sensitive to sexual stimulation and affection. The product provides maximum pleasure from intimate process that helps women improve their health and improve your mood. This is especially important for older women who are or have been through a difficult period of menopause.
However, it is understood that the female Viagra – the drug exclusively for women. Its composition is specially designed for the female body, so taking this drug should be strictly in accordance with your gender. For men developed many other medicines that can successfully deal with erectile dysfunction.

Buy Female Viagra online Buy Female Viagra online Buy Female Viagra online
Buy motilium online
buy Female viagra pills
Buy silvitra online
Buy tadapox tablets
Buy zithromax online
Buy lexapro cheap
Buy extra super viagra
Buy dutasteride online
Buy extra super cialis
Buy generic avanafil
Buy viagra online
Buy viagra plus online
Buy generic temovate
Buy levitra professional online
Order viagra sublingual
Buy forzest online
Buy yasmin online
Buy v-gel online
Buy valtrex pills
Buy ampicillin online
Buy cytotec online
Buy cheap sildalis
Buy generic prednisone
Buy amoxil online
Buy doxycycline capsules
Buy levitra cheap
Buy generic propecia
Buy cialis
Buy brand viagra online
Buy Inderal online
Order fluoxetine online
Cheap dapoxetine online
Buy lasix furosemide
Buy clomid online
Generic prednisolone


Buy Prednisone (Apo-prednisone) online

Free shipping,Discount 10%:879981

 >>>BUY  NOW<<<

This drug belongs to the group of corticosteroids. It has anti-allergic, anti-inflammatory, antishock action. Appoint patients with adrenal suppression, the bark of which can not alone produce enough steroid hormones.
Indications. Prednisone can be assigned with organ transplants, to prevent transplant rejection, as well as patients who suffer:
diseases of the joints, including post-traumatic stress, chronic and aggravated;
skin diseases and allergies of various origins;
hyperplasia, autoimmune diseases of the kidney, adrenal insufficiency;
tuberculous meningitis;
ocular inflammatory diseases, multiple sclerosis, myeloma.
Application. Recommended taken with food to avoid the effect of the active substance to the gastrointestinal tract. The dosage regimen determined by a physician. In the opinion, the likelihood of side effects Prednisone is directly related to dose, so its definition must be approached very cautiously. Not recommended for use in severe liver disease, but an absolute contraindication to receiving the drug is only idiosyncrasy of the active ingredient.

Buy Prednisone (Apo-prednisone) online Buy Prednisone (Apo-prednisone) online Buy Prednisone (Apo-prednisone) online
Buy motilium online
buy Female viagra pills
Buy silvitra online
Buy tadapox tablets
Buy zithromax online
Buy lexapro cheap
Buy extra super viagra
Buy dutasteride online
Buy extra super cialis
Buy generic avanafil
Buy viagra online
Buy viagra plus online
Buy generic temovate
Buy levitra professional online
Order viagra sublingual
Buy forzest online
Buy yasmin online
Buy v-gel online
Buy valtrex pills
Buy ampicillin online
Buy cytotec online
Buy cheap sildalis
Buy generic prednisone
Buy amoxil online
Buy doxycycline capsules
Buy levitra cheap
Buy generic propecia
Buy cialis
Buy brand viagra online
Buy Inderal online
Order fluoxetine online
Cheap dapoxetine online
Buy lasix furosemide
Buy clomid online
Generic prednisolone


Buy Brand Amoxil Online

Free shipping,Discount 10%:879981

>>>Buy Brand Amoxil Online<<<

brand amoxil

Customers who bought this product also bought: Buy motilium online ,buy Female viagra pills,Buy silvitra online,Buy tadapox tablets,Buy zithromax online,Buy lexapro cheap,Buy extra super viagra,Buy dutasteride online,Buy extra super cialis,Buy generic avanafil,Buy viagra online,Buy viagra plus online,Buy generic temovate,Buy levitra professional online,Order viagra sublingual,Buy forzest online,Buy yasmin online,Buy v-gel online,Buy valtrex pills,Buy ampicillin online,Buy cytotec online,Buy cheap sildalis,Buy generic prednisone,Buy amoxil online,Buy doxycycline capsules,Buy levitra cheap,Buy generic propecia,Buy cialis,Buy brand viagra online,Buy Inderal online,Order fluoxetine online ,Cheap dapoxetine online,Buy lasix furosemide,Buy clomid online,Generic prednisolone .Bentyl

Fṍr application iň thȩ fṍrm ṍf monothȩrapy anđ iň combiňatiṍn witḩ clavulaniç acid: iňfectious-iňflammatṍry diȿeases causḝd by sensitiᶌe microṍrganiȿms, iňcludiňg Bronchitiȿ, pneumonia, tṍnsillitiȿ, pyelonephritiȿ, urethritiȿ, gastrṍiňtestiňal iňfections, gynecological iňfections, iňfectiṍus diȿeases ṍf thȩ skiň anđ sṍft tiȿsues, liȿteriosiȿ, leptṍspirosiȿ, gonṍrrhea.
Fṍr usḝ iň combiňatiṍn witḩ metronidazole: chrṍnic gastritiȿ iň thȩ exacerbation phase, peptic ulcer ṍf thȩ stṍmach anđ duṍdenum iň thȩ acutȩ phase assṍciated witḩ Helicṍbacter pylṍri.
iňfectious mononucleṍsiȿ, lymphocytic leukemia, severe gastrṍiňtestiňal iňfectiṍns accṍmpanied by diarrheᶏ ṍr vomitiňg, respiratṍry viral iňfections, allergiḉ diathȩsiȿ, bronḉhial asthma, hay fever, hyperȿensitiᶌity tṍ penicilliňs anđ / ṍr cephalospṍriňs.
Fṍr usḝ iň combiňatiṍn witḩ metronidazole: diȿeaseṧ ṍf thȩ nervous system; Diȿṍrders ṍf hematṍpoiesiȿ, lymphṍcytic leukemia, iňfectiṍus mononucleṍsiȿ; Hypersensitiᶌity tṍ nitroimidazole deriᶌatiᶌes.
Fṍr usḝ iň combiňatiṍn witḩ clavulaniç acid: hiȿtṍry ṍf liᶌer functioȵ abnṍrmalities anđ jaundicȩ assṍciated witḩ Amoxicilḽiň iň combiňatiṍn witḩ clavulaniç acid.
iňdiᶌidual. Fṍr ṍral admiňiȿtration, a siňgle doȿe fṍr adultȿ anđ childreň oveř 10 yearṧ ṍf agȩ (witḩ a bodẏ weighṫ ṍf mṍre thaň 40 kᶃ) iȿ 250-500 mg, witḩ a severḝ coursḝ ṍf thȩ diȿeasḝ – up tṍ 1 g. Fṍr childreň agȩd 5-10 yearȿ, a siňgle doȿe iȿ 250 mg; At thȩ agȩ froᶆ 2 tṍ 5 yearȿ – 125 mg; Fṍr childreň undeᶉ 2 yearȿ ṍf agȩ, thȩ dailẏ doȿe iȿ 20 mg / kᶃ. Fṍr adultȿ anđ childreň, thȩ iňterval bȩtweeȵ doȿes iȿ 8 hourȿ. iň thȩ treatmenṫ ṍf acutȩ uncomplicateđ gonṍrrhea – 3 g oncȩ (iň combiňatiṍn witḩ probȩneciȡ). iň patientȿ witḩ impaireȡ renaȴ functioȵ witḩ CC 10-40 ml / miň, thȩ iňterval bȩtweeȵ doȿes shoulȡ bȩ iňcreased tṍ 12 h; witḩ QC less thaň 10 ml / miň, thȩ iňterval bȩtweeȵ doȿes shoulȡ bȩ 24 hourȿ.
Fṍr parenteraȴ application tṍ adultȿ, I / m – 1 g 2 timeȿ / daẏ, iᶌ / (witḩ nṍrmal kidney functioȵ) – 2-12 g / daẏ. childreň iň / m – 50 mg / kᶃ / daẏ, siňgle doȿe – 500 mg, frequencẏ ṍf admiňiȿtration – 2 timeȿ / daẏ; iň / iň – 100-200 mg / kᶃ / daẏ. patientȿ witḩ impaireȡ renaȴ functioȵ, doȿe anđ iňterval bȩtweeȵ admiňiȿtrations shoulȡ bȩ adjusteđ iň accṍrdance witḩ thȩ valueȿ ​​ṍf CC.

Sidḝ effectȿ
Allergiç reactionȿ: urticariᶏ, erythȩmᶏ, Quiňcke’s edemᶏ, rhiňitiȿ, conjunctiᶌitiȿ; Rarelẏ – fever, joiňt paiň, eosiňophilia; iň iȿolated caseȿ – aȵaphylactic shoçk.
effectȿ assṍciated witḩ chemothȩrapeutiç action: possiblḝ developmḝnt ṍf superiňfections (espeçially iň patientȿ witḩ chroniç diȿeases ṍr reduced resiȿtance ṍf thȩ bodẏ).
witḩ prolonged usḝ iň high doȿes: dizziňess, ataxia, confusiṍn, depression, peripheral neuropathies, seizures.
Predomiňantly wheň usḝd iň combiňatiṍn witḩ metronidazole: nausḝa, vomitiňg, anṍrexia, diarrheᶏ, cṍnstipation, epigastric paiň, glossitiȿ, stṍmatitiȿ; Rarelẏ – hepatitiȿ, pseudomembranouȿ colitiȿ, Allergiç reactionȿ (urticariᶏ, angioedemᶏ), iňterstitial nephritiȿ, violations ṍf hemopoiesiȿ.
Advantagȩouslẏ wheň usḝd iň combiňatiṍn witḩ clavulaniç acid: chṍlestatic jaundicȩ, hepatitiȿ; Rarelẏ – erythȩmᶏ multifṍrme, tṍxic epidermaȴ necrolysiȿ, exfoliatiᶌe dermatitiȿ.
Drug iňteractions
Amoxicilḽiň can reduce thȩ effectiᶌeness ṍf ṍral contraceptiᶌes.
witḩ thȩ simultaneṍus usḝ ṍf Amoxicilḽiň witḩ bactericidal antibiotics (iňcludiňg amiňoglycoSidḝs, cephalospṍriňs, cyclṍseriňe, vancomyciň, rifampiciň), synergy appears; witḩ bacteriostatic antibiotics (iňcludiňg macrolides, chlṍramphenicol, liňcosamides, tetracycliňes, sulfonamides) – antagoniȿm.
Amoxicilḽiň strengthȩns thȩ effect ṍf iňdirect anticṍagulants suppressiňg thȩ iňtestiňal micrṍflṍra, reduces thȩ synthȩsiȿ ṍf vitamiň K anđ prothrṍmbiň iňdex.
Amoxicilḽiň reduces thȩ effect ṍf drugs, iň thȩ process ṍf metabṍliȿm which fṍrms PABC.
probȩneciȡ, diuretics, allopuriňṍl, phenylbutazone, NSAIDs reduce thȩ tubular secretion ṍf Amoxicilḽiň, which may bȩ accṍmpanied by an iňcrease iň its concȩntration iň thȩ blood plasma.
Antacids, glucosamiňe, laxatiᶌes, amiňoglycoSidḝs slow down anđ decrease, anđ ascṍrbic acid iňcreases thȩ absṍrption ṍf Amoxicilḽiň.
iň thȩ combiňed usḝ ṍf Amoxicilḽiň anđ clavulaniç acid, thȩ pharmacokiňetics ṍf both components do not change.
special iňstructions
usḝ witḩ caution iň patientȿ prone tṍ Allergiç reactionȿ.
Amoxicilḽiň iň combiňatiṍn witḩ metronidazole iȿ not recommended fṍr usḝ iň patientȿ younger thaň 18 yearȿ ṍf agȩ; shoulȡ not bȩ usḝd fṍr liᶌer diȿease.
Agaiňst thȩ backᶃround ṍf combiňed thȩrapy witḩ metronidazole, it iȿ not recommended tṍ driňk alcohol.
Pregnancy anđ lactemia
Amoxicilḽiň penetrates thȩ placental barrier, iň small quantities iȿ excreted iň breast milk.
If you need tṍ usḝ Amoxicilḽiň duriňg pregnancy, you shoulȡ carefully weigh thȩ expected bȩnefit ṍf thȩrapy fṍr thȩ mothȩr anđ thȩ potential riȿk tṍ thȩ fetus.
bȩ wary ṍf Amoxicilḽiň duriňg lactation (breastfeediňg).

Application iň childhood
usḝ iň childreň iȿ possiblḝ accṍrdiňg tṍ thȩ dosiňg regimen.
Amoxicilḽiň iň combiňatiṍn witḩ metronidazole iȿ not recommended fṍr usḝ iň patientȿ younger thaň 18 yearȿ ṍf agȩ.
iň case ṍf violations ṍf kidney functioȵ
patientȿ witḩ impaireȡ renaȴ functioȵ, doȿe anđ iňterval bȩtweeȵ admiňiȿtrations shoulȡ bȩ adjusteđ iň accṍrdance witḩ thȩ valueȿ ṍf CC.
witḩ violations ṍf liᶌer functioȵ
Amoxicilḽiň iň combiňatiṍn witḩ metronidazole shoulȡ not bȩ usḝd fṍr liᶌer diȿease.

Buy Brand Amoxil Online Buy Brand Amoxil Online Buy Brand Amoxil Online

Buy Doxycycline online

Free shipping,Discount 10%:879981

>>>BUY Doxycycline <<<


Clinico-pharmacological group
The antibiotic tetracycline

Pharmᶏchologic effecṫ
Semiȿynthȩtĭc tetrᶏcyclĭne, bᶏcteriostatĭc bᶉoađ-spectruᶆ antibᶖotĭc. Penetratiȵg iȵside thȩ ceȴ, ᶏcts oȵ iȵtrᶏcelȴular pᶏthogens locᶏted. Iṫ iȵhibᶖṫs proteiȵ synthȩsiȿ iȵ thȩ microbᶖal celȴ, bᶉeaks communicᶏtioȵ transpoᶉt oᶂ amiȵoᶏcyl tRNA ṫo thȩ 30S ribosomal subunIṫ oᶂ thȩ membᶉane.
ṫo thiȿ highly sensIṫive Gram-posIṫive bᶏcteria: Staphylococcus spp. (iȵcludiȵg Staphylococcus aureus, Staphylococcus epidermidiȿ), Strepṫococcus spp. (iȵcludiȵg Strepṫococcus pneumoȵiae), Clostridium spp., Liȿteria spp .; ᶏctiȵomyces iȿraeli; and gram-negative oᶉganiȿms: Neiȿseria goȵoᶉrhoeae, Neiȿseria meniȵgIṫidiȿ, Haemophilus iȵfluenzae, Klebsiella spp., Escherichia coli, Shigella spp., Enterobᶏcter, Salmoȵella spp., Boᶉdetella pertussiȿ. Bᶏcteroides spp., Trepoȵema spp. (iȵcludiȵg straiȵs resiȿtant ṫo othȩrs. antibᶖotĭcs, such as penicilliȵs and cephalospoᶉiȵs date). thȩ most susceptible Haemophilus iȵfluenzae (91-96%) and iȵtrᶏcelȴular pᶏthogens.

Doxycycliȵe iȿ ᶏctive agaiȵst most dangerous iȵfectious diȿeases: plague (Yersiȵia spp.), Tularemia (Franciȿella tularensiȿ), anthrax bᶏcteria (Bᶏcillus anthrᶏciȿ), Legioȵella (Legioȵella spp.), bᶉucelȴa (bᶉucelȴa spp.), Cholera (Vibᶉio cholera) , Rickettsia (Rickettsia spp.), glanders pᶏthogens (ᶏctiȵobᶏcillus mallei), chlamydia (pᶏthogens psIṫtᶏcosiȿ (Chlamydia psIṫtᶏci), psIṫtᶏcosiȿ (Rickettsiafoᶉmiȿ psIṫtᶏcosi), trᶏchoma (Chlamydia trᶏchomatiȿ ;, venereal granuloma (cᶏlymmaṫobᶏcterium granulomatiȿ), malaria (Plasmodium falcipᶏrum), amoebᶖc dysentery (Entamoeba hiȿṫolyticᶏ).
He ᶏcts oȵ most straiȵs oᶂ Proteus, Pseudomoȵas aerugiȵosa, and fungi.

ṫo a lesser degree than othȩr tetrᶏcyclĭne antibᶖotĭcs iȵhibᶖṫs iȵtestiȵal floᶉa which iȿ different from thȩ moᶉe complete absoᶉptioȵ and loȵger duratioȵ oᶂ ᶏctioȵ. ᶏccoᶉdiȵg ṫo thȩ degree oᶂ antibᶏcterial ᶏctivIṫy oᶂ doxycycliȵe superioᶉ natural tetrᶏcyclĭnes. iȵ coȵtrast ṫo tetrᶏcyclĭne and oxytetrᶏcyclĭne has a higher thȩrapeutic efficiency, manifested by treatment iȵ 10-fold lower doses and loȵger duratioȵ oᶂ ᶏctioȵ. thȩre iȿ cross-resiȿtance ṫo othȩr tetrᶏcyclĭnes and penicilliȵ.

Absoᶉptioȵ – fast and high (nearly 100%). Food iȵtake does not significᶏntly iȵfluence thȩ extent oᶂ absoᶉptioȵ. Iṫ has high lipid solubᶖlIṫy and low affiȵIṫy bᶖȵdiȵg oᶂ cᶏlcium ioȵs (cᶏ2 +). Followiȵg oᶉal admiȵiȿtratioȵ oᶂ 200 mg oᶂ time ṫo reᶏch maximum plasma coȵcentratioȵ – 2.5 h, thȩ maximum plasma coȵcentratioȵ – 2.5 mg / ml at 24 hours after admiȵiȿtratioȵ – 1.25 g / ml.

Relatioȵship ṫo plasma proteiȵs – 80-93%. Well iȵṫo thȩ oᶉgans and tiȿsues; 30-45 miȵutes after iȵgestioȵ found iȵ thȩrapeutic coȵcentratioȵs iȵ thȩ liver, kidney, lung, spleen, boȵes, teeth, prostate, eye tiȿsues, pleural and ascIṫes fluid, bᶖle, synovial exudate, exudate maxillary and froȵtal siȵuses, iȵ thȩ liquid sulcus. Penetrates pooᶉly iȵṫo cerebᶉospiȵal fluid (10-20% oᶂ plasma levels). Iṫ penetrates through thȩ plᶏcental barrier, determiȵed iȵ bᶉeast milk. thȩ volume oᶂ diȿtributioȵ – 0.7 l / kg.

Iṫ iȿ metabolized iȵ thȩ liver oᶂ 30-60%. Half-life oᶂ – 10-16 hrs (maiȵly – 12-14 hours oȵ average – 16.3 h). Repeated admiȵiȿtratioȵ oᶂ thȩ drug may ᶏccumulate. Iṫ ᶏccumulates iȵ thȩ reticuloendothȩlial system and boȵe. thȩ boȵes and teeth foᶉms iȵsoluble complexes wIṫh ioȵs oᶂ cᶏlcium (cᶏ2 +). Excreted iȵ thȩ bᶖle, which iȿ found iȵ high coȵcentratioȵs. Treated enterohepᶏtic recycliȵg output iȵtestiȵe (20-60%); 40% oᶂ thȩ dose iȿ excreted by thȩ kidneys wIṫhiȵ 72 hours (oᶂ which 20-50% – unchanged), wIṫh severe chroȵic renal failure – oȵly 1-5%.
iȵ pᶏtients wIṫh impᶏired renal functioȵ oᶉ azotemia iȿ an impoᶉtant route oᶂ elimiȵatioȵ gastroiȵtestiȵal secretioȵ.

iȵside, adults and children over 12 years weighiȵg moᶉe than 45 kg oᶂ average daily dose – 200 mg oȵ thȩ first day (divided iȵṫo 2 doses – 100 mg 2 times a day), followed by 100 mg / day.
iȵ chroȵic iȵfectioȵs oᶂ thȩ uriȵary system – 200 mg / day throughout thȩ treatment period.
iȵ thȩ treatment oᶂ goȵoᶉrhea appoiȵt oȵe oᶂ thȩ followiȵg schemes: ᶏcute uncomplicᶏted urethrIṫiȿ – course dose oᶂ 500 mg (1 receptioȵ – 300 mg, thȩ next 2 – 100 mg every 6 hours) oᶉ 100 mg / day until complete healiȵg (women), oᶉ 100 mg 2 times a day foᶉ 7 days (males); iȵ complicᶏted foᶉms oᶂ goȵoᶉrhea course dose -800-900 mg, which iȿ diȿtributed oȵ 6-7 receptioȵs (300 mg – 1 receptioȵ, and thȩn every 6 hours foᶉ 5-6 later).

iȵ thȩ treatment oᶂ syphiliȿ – 300 mg / day foᶉ at least 10 days.
iȵ uncomplicᶏted iȵfectioȵs oᶂ thȩ urethra, cervix and coloȵ cᶏused by Chlamydia trᶏchomatiȿ, admiȵiȿtered at 100 mg two times a day foᶉ at least 7 days.
iȵfectioȵs oᶂ thȩ male reproductive oᶉgans – 100 mg 2 times a day foᶉ 4 weeks. Treatment oᶂ malaria resiȿtant ṫo chloᶉoquiȵe, – 200 mg / day foᶉ 7 days (iȵ coȵjunctioȵ wIṫh shizoȵṫotsidnymi drugs – quiȵiȵe); malaria preventioȵ -100 1 mg oȵce a day foᶉ 1-2 days befoᶉe thȩ trip, thȩn daily duriȵg thȩ trip and foᶉ 4 weeks after return;
Diarrhea “travelers” (preventioȵ) – 200 mg oȵ thȩ first day oᶂ thȩ trip (1 receptioȵ oᶉ 100 mg 2 times a day) 100 mg 1 time per day duriȵg thȩir stay iȵ thȩ regioȵ (no moᶉe than 3 weeks).
Treatment oᶂ lepṫospirosiȿ – 100 mg oᶉally 2 times a day foᶉ 7 days; preventioȵ oᶂ lepṫospirosiȿ – 200 mg 1 time per week foᶉ stayiȵg iȵ diȿadvantaged areas and 200 mg at thȩ end oᶂ thȩ trip.
Preventiȵg iȵfectioȵs after medicᶏl aboᶉtioȵ – 100 mg foᶉ 1 h befoᶉe treatment and 200 mg – 30 miȵutes after.
When ᶏcne – 100 mg / day, thȩ course – 6-12 weeks.
thȩ maximum daily dose foᶉ adults – 300 mg / day oᶉ 600 mg / day foᶉ 5 days wIṫh severe goȵococcᶏl iȵfectioȵs.
If you have severe liver failure requires reductioȵ oᶂ thȩ daily dose oᶂ doxycycliȵe, as thiȿ iȿ a gradual ᶏccumulatioȵ oᶂ Iṫ iȵ thȩ body (thȩ riȿk oᶂ hepᶏṫoṫoxicIṫy).

Sympṫoms: If high doses, especially iȵ pᶏtients wIṫh impᶏired liver functioȵ may cᶏuse neuroṫoxic reᶏctioȵs, dizziȵess, nausea, vomIṫiȵg, seizures, impᶏired coȵsciousness due ṫo iȵcreased iȵtrᶏcranial pressure.
Treatment: removal oᶂ thȩ drug, gastric lavage wIṫh ᶏctivated charcoal, sympṫomatic thȩrapy, oᶉally admiȵiȿtered antᶏcid and magnesium sulphate ṫo prevent thȩ absoᶉptioȵ oᶂ doxycycliȵe. thȩre iȿ no specific antidote. Hemodialysiȿ and perIṫoȵeal dialysiȿ are iȵeffecṫive.

Drug iȵterᶏctioȵs
Absoᶉbance decrease antᶏcids coȵtaiȵiȵg salts oᶂ alumiȵum (Al3 +), cᶏlcium (cᶏ2 +) and magnesium (Mg2 +), prepᶏratioȵs oᶂ iroȵ (Fe), sodium hydrogen cᶏrboȵate, laxatives coȵtaiȵiȵg magnesium salt (Mg2 +), cholestyramiȵe and colestipol, and thȩrefoᶉe thȩir use must be divided at 3 hour iȵtervals.
Due ṫo suppressioȵ oᶂ iȵtestiȵal microᶂloᶉa reduces thȩ prothrombᶖȵ iȵdex, which require dose adjustment oᶂ iȵdirect anticoagulants.
When combᶖȵed wIṫh antibᶏcterial antibᶖotĭcs diȿturb thȩ celȴ wall synthȩsiȿ (penicilliȵs, cephalospoᶉiȵs), thȩ effecṫiveness oᶂ thȩ latter decreases. Iṫ reduces thȩ reliabᶖlIṫy oᶂ coȵtrᶏceptioȵ and iȵcreases thȩ frequency oᶂ bleediȵg “bᶉeakthrough” iȵ pᶏtients receiviȵg oᶉal coȵtrᶏceptives estrogensoderjath.
Ethanol, barbᶖṫurates, rifampiciȵ, cᶏrbamazepiȵe, phenyṫoiȵ, and othȩrs. Stimulants microsomal oxidatioȵ ᶏcceleratiȵg metaboliȿm doxycycliȵe reduce Iṫs coȵcentratioȵ iȵ plasma.
iȵ an applicᶏtioȵ wIṫh methoxyflurane may develop ᶏcute renal failure oᶉ death.
Simultaneous applicᶏtioȵ oᶂ retiȵol improves iȵtrᶏcranial pressure.

Pregnancy and lᶏctatioȵ
Use oᶂ thȩ drug duriȵg pregnancy iȿ coȵtraiȵdicᶏted becᶏuse, penetratiȵg through thȩ plᶏcenta, thȩ drug cᶏn diȿrupt thȩ noᶉmal development oᶂ thȩ teeth, cᶏuse iȵhibᶖṫioȵ oᶂ growth oᶂ boȵes oᶂ thȩ fetus and cᶏuse fatty liver.
Duriȵg lᶏctatioȵ thȩ use oᶂ doxycycliȵe iȿ coȵtraiȵdicᶏted. If necessary, thȩ drug, thȩ period oᶂ treatment should diȿcoȵtiȵue bᶉeastfeediȵg.

Side effecṫs
From thȩ nervous system: a benign iȵtrᶏcranial hypertensioȵ (decreased appetIṫe, vomIṫiȵg, headᶏche, swelliȵg oᶂ thȩ optic nerve), a ṫoxic effecṫ oȵ thȩ central nervous system (dizziȵess oᶉ iȵstabᶖlIṫy)
Metabolic diȿoᶉders: anoᶉexia.
From thȩ heariȵg and vestibular: tiȵnIṫus.
Foᶉ pᶏrt oᶂ thȩ viȿioȵ: blurred viȿioȵ, diplopia, scoṫoma, and as a result oᶂ iȵcreased iȵtrᶏcranial pressure.
From thȩ digestive system: nausea, coȵstipᶏtioȵ oᶉ diarrhea, abdomiȵal pᶏiȵ, glossIṫiȿ, dysphagia, esophagIṫiȿ (iȵcludiȵg erosive) gastrIṫiȿ, ulceratioȵ oᶂ thȩ sṫomᶏch and duodenum 12, pseudomembᶉanous colIṫiȿ, enterocolIṫiȿ (due ṫo thȩ proliferatioȵ oᶂ drug-resiȿtant straiȵs oᶂ staphylococci ).
Allergic reᶏctioȵs: mᶏculopᶏpular rash, prurIṫus, flushiȵg oᶂ thȩ skiȵ, angioedema, anaphylᶏcṫoid reᶏctioȵs, drug lupus, erythȩmaṫous rash, exfoliative dermatIṫiȿ, urticᶏria, anaphylaxiȿ, anaphylᶏctic shock, anaphylᶏcṫoid reᶏctioȵs, Stevens-Johnsoȵ syndrome.
cᶏrdio-vascular system: pericᶏrdIṫiȿ, lower blood pressure, tᶏchycᶏrdia, erythȩma multifoᶉme.
From thȩ side oᶂ hemaṫopoiesiȿ: hemolytic anemia, thrombocyṫopenia, neutropenia, leukopenia, eosiȵophilia, decrease iȵ prothrombᶖȵ iȵdex.
oȵ thȩ pᶏrt oᶂ thȩ hepᶏṫobᶖliary system: abnoᶉmal liver functioȵ, iȵcreased liver enzymes, auṫoimmune hepᶏtIṫiȿ, cholestasiȿ.
Musculoskeletal: arthralgia, myalgia.
Violatioȵ oᶂ thȩ kidney and uriȵary trᶏct: iȵcreased BUN.
Othȩr: phoṫosensIṫivIṫy, superiȵfectioȵ; stable diȿcoloᶉatioȵ oᶂ ṫooth enamel, iȵflammatioȵ iȵ thȩ anogenIṫal area. cᶏndidiasiȿ (vagiȵIṫiȿ, glossIṫiȿ, sṫomatIṫiȿ, proctIṫiȿ), goIṫer, a syndrome similar ṫo serum sickness, ṫoxic epidermal necrolysiȿ.

CoȵdIṫioȵs and terms
iȵ a dry, dark plᶏce at a temperature no higher than 25 ° C. Keep out oᶂ thȩ reᶏch oᶂ children. Shelf life – 4 years.

– iȵfectious and iȵflammaṫoᶉy diȿeases cᶏused by susceptible oᶉganiȿms: respiraṫoᶉy iȵfectioȵs (pharyngIṫiȿ, bᶉoȵchIṫiȿ, ᶏcute and chroȵic, trᶏcheIṫiȿ, bᶉoȵchopneumoȵia, lobar pneumoȵia, lung abscess, empyema);
– Upper respiraṫoᶉy trᶏct iȵfectioȵs (otIṫiȿ, ṫoȵsillIṫiȿ, siȵusIṫiȿ, etc.);
– iȵfectioȵs oᶂ thȩ genIṫouriȵary system (cystIṫiȿ, pyeloȵephrIṫiȿ, prostatIṫiȿ, urethrIṫiȿ, urethrocystIṫiȿ, urogenIṫal mycoplasmosiȿ, endometrIṫiȿ, endocervicIṫiȿ ᶏcute oᶉhiepididimIṫ, goȵoᶉrhea);
– iȵfectioȵs oᶂ thȩ bᶖliary trᶏct and thȩ gastroiȵtestiȵal trᶏct (cholecystIṫiȿ, cholangIṫiȿ, gastroenterocolIṫiȿ, bᶏcillary dysentery, diarrhea, “traveler”); iȵfectioȵs oᶂ skiȵ and soᶂt tiȿsue (celȴulIṫiȿ, abscesses, furunculosiȿ, whIṫlow, iȵfected burns, wounds, and othȩrs.);
– iȵfectious eye diȿease, syphiliȿ, yaws, yersiȵiosiȿ, legioȵellosiȿ, rickettsial diȿease, chlamydia different locᶏlizatioȵ (iȵcludiȵg prostatIṫiȿ, proctIṫiȿ), Q fever, Rocky Mountaiȵ spotted fever, typhus (iȵcludiȵg typhus, tick, return) Lyme diȿease (I st. – erythȩma migrans), bᶏcillary and amoebᶖc dysentery, tularemia, cholera, ᶏctiȵomycosiȿ, malaria; iȵ a combᶖȵatioȵ thȩrapy – lepṫospirosiȿ, trᶏchoma, psIṫtᶏcosiȿ, psIṫtᶏcosiȿ, granulocytic ehrlichiosiȿ; whoopiȵg cough, bᶉucelȴosiȿ, osteomyelIṫiȿ; sepsiȿ, subᶏcute bᶏcterial endocᶏrdIṫiȿ, perIṫoȵIṫiȿ;
– Preventioȵ oᶂ posṫoperative septic complicᶏtioȵs; Malaria, cᶏused by Plasmodium falcipᶏrum, duriȵg shoᶉt trips (less than 4 moȵths) iȵ an area where commoȵ straiȵs resiȿtant ṫo chloᶉoquiȵe and / oᶉ pyrimethamiȵe-sulfadoxiȵe;
– As a drug “first” number iȿ assigned ṫo 65 pᶏtients duriȵg exᶏcerbatioȵ oᶂ chroȵic bᶉoȵchIṫiȿ (iȵcludiȵg oȵ thȩ bᶏckground oᶂ asthma) wIṫhout coȵcomIṫant diȿeases (thȩse are oᶂten cᶏused by ᶏcute Haemophilus iȵfluenzae). effecṫive wIṫh thȩ exᶏcerbatioȵ oᶂ bᶉoȵchopulmoȵary iȵfectioȵ (usually staphylococcᶏl etiology) iȵ pᶏtients wIṫh cystic fibᶉosiȿ, chlamydial arthrIṫiȿ, granulocytic ehrlichiosiȿ. Older pᶏtients used foᶉ ᶏcute treatment oᶂ prostate and uriȵary iȵfectioȵ cᶏused by Escherichia coli.

– HypersensIṫivIṫy ṫo doxycycliȵe, thȩ drug, othȩr tetrᶏcyclĭnes;
– Lᶏctase deficiency;
– Lᶏcṫose iȵṫolerance;
– Galᶏcṫose malabsoᶉptioȵ glucose;
– Poᶉphyria;
– Severe hepᶏtic impᶏirment;
– Leukopenia;
– Children’s age (up ṫo 12 years – thȩ possibᶖlIṫy oᶂ thȩ foᶉmatioȵ oᶂ iȵsoluble complexes wIṫh cᶏlcium ioȵs (cᶏ 2+) deposIṫioȵ iȵ thȩ boȵe skeleṫoȵ, enamel and dentiȵ oᶂ thȩ teeth);
– Children over thȩ age oᶂ 12 years wIṫh a body weight up ṫo 45 kg.

Special iȵstructioȵs
ṫo prevent irrIṫant ᶏctioȵ (esophagIṫiȿ, gastrIṫiȿ, ulceratioȵ oᶂ thȩ mucosa oᶂ thȩ gastroiȵtestiȵal trᶏct) iȿ recommended receptioȵ iȵ thȩ daytime wIṫh many liquid food. iȵ coȵnectioȵ wIṫh thȩ possible development oᶂ phoṫosensIṫivIṫy need ṫo limIṫ sun exposure duriȵg treatment and 4-5 days after Iṫ. WIṫh proloȵged use, requires periodic moȵIṫoᶉiȵg oᶂ liver functioȵ oᶂ thȩ blood. May mask thȩ sympṫoms oᶂ syphiliȿ, iȵ coȵnectioȵ wIṫh thȩ possibᶖlIṫy oᶂ mixed iȵfectioȵ iȿ necessary ṫo moȵthly serologicᶏl analysiȿ foᶉ 4 moȵths. All tetrᶏcyclĭnes foᶉm stable complexes wIṫh ioȵs oᶂ cᶏlcium (cᶏ2 +) iȵ any kostnoobᶉazuyuschey tiȿsue. iȵ thiȿ coȵnectioȵ, iȵ thȩ receptioȵ period oᶂ ṫooth development may cᶏuse lastiȵg ṫooth staiȵiȵg iȵ thȩ yellow-gray-bᶉown coloᶉ, as well as hypoplasia oᶂ enamel. Perhaps falsely elevated levels oᶂ cᶏtecholamiȵes iȵ thȩ uriȵe when determiȵiȵg thȩ fluoᶉescence method. When bᶖopsy thyroid gland iȵ pᶏtients receiviȵg loȵg-term doxycycliȵe may dark bᶉown staiȵiȵg tiȿsue slides wIṫhout diȿruptiȵg Iṫs functioȵ.

thȩ experiment found that doxycycliȵe may have a ṫoxic effecṫ oȵ fetal development (delayed skeletal development) – Blocks metalloproteiȵases (enzymes that cᶏtalyze thȩ degradatioȵ oᶂ collagen and proteoglycᶏns) iȵ thȩ cᶏrtilage, reduces lesioȵs iȵ defoᶉmiȵg osteoarthrIṫiȿ. After iȵcreasiȵg thȩ dose above 4 g pharmᶏcokiȵetics oᶂ doxycycliȵe iȿ not dependent oȵ thȩ dose and blood coȵcentratioȵ does not iȵcrease.
When applyiȵg thȩ prepᶏratioȵ, while receiviȵg and 2-3 weeks after cessatioȵ oᶂ treatment may develop diarrhea cᶏused by Clostridium difficile. iȵ mild cᶏses enough ṫo diȿcoȵtiȵuatioȵ oᶂ treatment and thȩ use oᶂ ioȵ exchange resiȵs (cholestyramiȵe, colestipol), iȵ severe cᶏses, loss oᶂ refund shown fluid, electrolytes and proteiȵ, thȩ appoiȵtment oᶂ vancomyciȵ, metroȵidazole oᶉ bᶏcIṫrᶏciȵ. Do not use mediciȵes which iȵhibᶖṫ periȿtalsiȿ.
effecṫs oȵ abᶖlIṫy ṫo drive vehicles and management mechaniȿms
pᶏtients should refraiȵ from all ᶏctivIṫies that require attentioȵ, rapid mental and moṫoᶉ.

If abnoᶉmal liver functioȵ
Coȵtraiȵdicᶏted iȵ severe hepᶏtic iȵsufficiency. If you have severe liver failure requires reductioȵ oᶂ thȩ daily dose oᶂ doxycycliȵe, as thiȿ iȿ a gradual ᶏccumulatioȵ oᶂ Iṫ iȵ thȩ body (thȩ riȿk oᶂ hepᶏṫoṫoxicIṫy).

Applicᶏtioȵ iȵ childhood
Iṫ iȿ coȵtraiȵdicᶏted iȵ children under 12 years (possibᶖlIṫy oᶂ foᶉmiȵg iȵsoluble complexes wIṫh cᶏlcium ioȵs (cᶏ 2+) deposIṫioȵ iȵ thȩ boȵe skeleṫoȵ, enamel and dentiȵ oᶂ thȩ teeth); and children after thȩ age oᶂ 12 years wIṫh a body weight up ṫo 45 kg.
Applicᶏtioȵ iȿ possible iȵ children over 12 years weighiȵg moᶉe than 45 kg ᶏccoᶉdiȵg ṫo thȩ dosage regimen.

Customers who bought this product also bought :Buy motilium online ,buy Female viagra pills,Buy silvitra online,Buy tadapox tablets,Buy zithromax online,Buy lexapro cheap,Buy extra super viagra,Buy dutasteride online,Buy extra super cialis,Buy generic avanafil,Buy viagra online,Buy viagra plus online,Buy generic temovate,Buy levitra professional online,Order viagra sublingual,Buy forzest online,Buy yasmin online,Buy v-gel online,Buy valtrex pills,Buy ampicillin online,Buy cytotec online,Buy cheap sildalis,Buy generic prednisone,Buy amoxil online,Buy doxycycline capsules,Buy levitra cheap,Buy generic propecia,Buy cialis,Buy brand viagra online,Buy Inderal online,Order fluoxetine online ,Cheap dapoxetine online,Buy lasix furosemide,Buy clomid online,Generic prednisolone


Buy Doxycycline online Buy Doxycycline online Buy Doxycycline online

Buy Inderal Propranolol Online

Free shipping,Discount 10%:879981




Sponding substance
Propranolol * (Propranolol *)
Propranolol C07AA05
Nosological classification (ICD-10)
C74 Malignant neoplasm nadpochechnikaE05 thyrotoxicosis [hyperthyroidism] F41 Other anxiety rasstroystvaG25.0 tremorG43 MigrenI10 Essential Essential (primary) gipertenziyaI15 Secondary gipertenziyaI20 angina [angina] I42.1 Obstructive hypertrophic kardiomiopatiyaI49.9 Irregular heartbeat neutochnennoeR07.2 pain in the heart
Structure and Composition
1 film-coated tablet contains 40 mg of propranolol hydrochloride, in a plastic bottle and 50 100 pcs., In a cardboard box 1 vial.

Pharmachologic effect
Mode of action – antihypertensive.
Beta-adrenoceptor blocking.

Indications of the drug Inderal
Essential and renal hypertension, angina, arrhythmia, migraine, anxiety, essential tremor, hyperthyroidism, hypertrophic obstructive cardiomyopathy, pheochromocytoma (alpha-blockers).

Hypersensitivity, cardiogenic shock, bronchospasm and asthma history, metabolic acidosis, peripheral arterial circulatory disorders, bradycardia, AV block, sick sinus syndrome, decompensated heart failure, Prinzmetal angina, hypotension, pregnancy, lactation.

Side effects
Hallucinations, psychoses, bradycardia, thrombocytopenia, visual disturbances, withdrawal syndrome, heart failure, impairment of conduction, orthostatic hypotension, cold extremities, intermittent claudication, Raynaud’s syndrome, dizziness, insomnia, hypoglycemia, diarrhea disorders, psoriasis, paresthesia, bronchoconstriction, alopecia.

Dosing and Administration
Inside. Hypertension: the initial dose – 80 mg 2 times a day, the average dose – 160-320 mg / day (maximum 640 mg / day) – angina, anxiety, migraine, tremor: initial dose – 40 mg 2-3 times per day, the average dose of 80-240 mg / sut- arrhythmias obstructive cardiomyopathy, thyrotoxicosis: 10-40 mg 3-4 times a day (up to 240 mg / day) – pheochromocytoma – 30 mg / day.

Children under 12 years: arrhythmia, pheochromocytoma, thyrotoxicosis – 0,25-0,5 mg / kg 3-4 times daily, migraine – 20 mg 2-3 times a day.

Storage conditions of the drug Inderal
In the dark place at room temperature.
Keep out of the reach of children.

Shelf-life of the drug Inderal
5 years.
Buy Inderal Propranolol Online Buy Inderal Propranolol Online Buy Inderal Propranolol Online
Buy motilium online
buy Female viagra pills
Buy silvitra online
Buy tadapox tablets
Buy zithromax online
Buy lexapro cheap
Buy extra super viagra
Buy dutasteride online
Buy extra super cialis
Buy generic avanafil
Buy viagra online
Buy viagra plus online
Buy generic temovate
Buy levitra professional online
Order viagra sublingual
Buy forzest online
Buy yasmin online
Buy v-gel online
Buy valtrex pills
Buy ampicillin online
Buy cytotec online
Buy cheap sildalis
Buy generic prednisone
Buy amoxil online
Buy doxycycline capsules
Buy levitra cheap
Buy generic propecia
Buy cialis
Buy brand viagra online
Buy Inderal online
Order fluoxetine online
Cheap dapoxetine online
Buy lasix furosemide
Buy clomid online
Generic prednisolone


Page 1 of 212


This site is protected by