Vendiol 0.06mg / 0.015mg, 28 tablets — Made in Hungary — Free Delivery
(Vendiol)
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Description Vendiol 0.06mg / 0.015mg, 28 tablets — Made in Hungary — Free Delivery
Product description
Vendiol tablets are used for hormonal oral contraception. When deciding on the appointment of the preprarion "Vendiol", it is necessary to take into account the current risk factors for the individual woman, especially the risk factors for venous thromboembolism (VTE), and how high the risk of VTE is with the use of the preprarion "Vendiol" compared with other combined hormonal contraceptives.
Compound
Active ingredients: gestodene, ethinylestradiol.
One active tablet contains:
active ingredients: gestodene 0.060 mg (micronized) and ethinylestradiol 0.015 mg (micronized);
excipients: lactose monohydrate, microcrystalline cellulose (type 112), potassium polacrilin, magnesium stearate;
film shell: Opadry II yellow 31K32378, lactose monohydrate, hypromellose (type 2910), titanium dioxide (E 171), triacetin, quinoline yellow dye (E 104).
One placebo tablet contains:
active ingredients: absent;
excipients: microcrystalline cellulose, anhydrous lactose, pregelatinized corn starch, magnesium stearate, anhydrous colloidal silicon dioxide;
film shell: Opadry II green 85F21389, polyvinyl alcohol, titanium dioxide (E 171), macrogol 3350, talc, indigo carmine dye (E 132), quinoline yellow dye (E 104), iron oxide black dye (E 172), sunset yellow dye (E 110).
Contraindications
Combined hormonal contraceptives (CHCs) should not be used in the following cases. If any of these conditions occur while using a COC, you should immediately stop taking it.
Hypersensitivity to the active substances or to any of the excipients.
Presence or risk of venous thromboembolism (VTE):
- venous thromboembolism - there is a VTE (use of anticoagulants) or a history of VTE (for example, deep vein thrombosis (DVT) or pulmonary embolism (PE)); known hereditary or acquired tendency to venous thromboembolism, for example, resistance to activated protein C (APC, including factor V Leiden), antithrombin-III deficiency, protein C deficiency, protein S deficiency;
- significant surgical intervention with prolonged immobilization;
- high risk of venous thromboembolism due to the presence of multiple risk factors.
- Presence or risk of arterial thromboembolism (ATE):
- arterial thromboembolism - there is an arterial thromboembolism, a history of arterial thromboembolism (eg, myocardial infarction) or a prodromal condition (eg, angina pectoris);
- cerebrovascular disease - there is a stroke, a history of stroke, a prodromal condition (for example, transient ischemic attack (TIA));
- known hereditary or acquired tendency to arterial thromboembolism, for example, hyperhomocysteinemia and antiphospholipid antibodies (anticardiolipin antibodies, lupus anticoagulant);
- migraine with a history of focal neurological symptoms;
- high risk of arterial thromboembolism as a result of multiple risk factors or the presence of any of the following major risk factors:
- diabetes mellitus with vascular complications;
- severe arterial hypertension;
- severe dyslipidemia;
- the presence of a malignant neoplasm of the mammary glands or suspicion of it;
- endometrial carcinoma or the presence of any other estrogen-dependent tumor or suspicion of it; the presence of liver tumors (benign or malignant) or a history of such tumors, severe liver disease (until liver function is restored);
- severe renal failure or acute renal failure;
- bleeding from the vagina of unknown etiology;
- the presence of pancreatitis or a history of pancreatitis if it is associated with severe hypertriglyceridemia.
Mode of application
For oral administration.
Swallow the tablets whole without chewing, if necessary, with a small amount of liquid every day at about the same time in the order indicated on the blister pack. Take one tablet per day (preferably at the same time of day) for 28 consecutive days (one yellow tablet per day for 24 days, then one green placebo tablet per day for the next 4 days) without a break between taking the tablets from the next package. Withdrawal bleeding usually begins 2-3 days after the last tablet containing the active substance and may continue until the start of taking the tablets from a new package.
This is an introductory part of the instructions, read the full instructions inside the package.
Application features
pregnant
"Vendiol" is contraindicated for use during pregnancy.
The use of this preprarion is not recommended during breastfeeding, as estrogen and progestogen pass into breast milk, which can adversely affect the baby.
Children
The preprarion is not intended for use in children.
Drivers
"Vendiol" does not affect or has a slight effect on the ability to drive vehicles and mechanisms.
Overdose
No serious side effects have been observed as a result of taking large doses of COCs. General experience with the use of COCs suggests that such cases may be accompanied by the following symptoms: nausea, vomiting, and in young girls - minor vaginal bleeding.
There is no specific antidote, so treatment should be purely symptomatic.
Side effects
The use of any COC increases the risk of VTE. In clinical studies, amenorrhea was found in 15% of patients. The most common side effects reported by patients in phase III clinical trials and in the post-marketing period were headache, migraine, bleeding, and spotting.
This is an introductory part of the instructions, read the full instructions inside the package.
Storage conditions
Store in the original packaging to protect from light and moisture at a temperature not exceeding 30°C, out of the reach of children.
Shelf life - 2 years.
Tags: Vendiol
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