Product image of Hastina 21+7 (Drospirenone, Ethinylestradiol | Lactose Anhydrous) supplied by GNH India

Hastina 21+7

Active Ingredient:
Drospirenone, Ethinylestradiol | Lactose Anhydrous
Origin:
EU

Hastina 21+7 (Drospirenone, Ethinylestradiol | Lactose Anhydrous)

Hastina 21+7 is a combined oral contraceptive tablet containing the synthetic progestogen drospirenone and the estrogen ethinylestradiol. Marketed in the European Union, it is taken orally and includes lactose anhydrous as an inactive ingredient. The product is classified as a hormonal contraceptive and is prescribed for the prevention of pregnancy, typically following a 21‑day active phase with a 7‑day hormone‑free interval under medical supervision and regular follow‑up.

Manufacturer / TM Owner

Aristo Pharma Sp. Z O.O.

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Indications & Clinical Uses

Hastina 21+7 is indicated for women who seek reliable hormonal contraception.

  • Prevention of pregnancy in women of reproductive age.
  • Use as part of a regular 21‑day active/7‑day placebo cycle.
  • May be prescribed for menstrual cycle regulation when clinically appropriate.
  • Can be considered for management of acne related to androgen excess in some patients.
  • Provides contraceptive protection immediately after the first tablet when a backup method is not required after the first 7 days.

Side Effects

Like other combined oral contraceptives, Hastina 21+7 may cause a range of side effects, most of which are mild and transient.

Common

  • Nausea or mild stomach upset, often occurring during the first cycle.
  • Headache or mild migraine, which may improve after continued use.
  • Breast tenderness or enlargement, typically resolving after several weeks.
  • Spotting or breakthrough bleeding between periods, especially during the initial weeks.

Serious

  • Signs of venous thromboembolism such as leg pain, swelling, redness, or sudden shortness of breath, which require immediate medical attention.
  • Severe allergic reaction including rash, itching, swelling of the face, lips, tongue, or throat, indicating possible anaphylaxis.

Precautions & Warnings

Before prescribing Hastina 21+7, clinicians evaluate several health factors to ensure safe use.

  • History of blood clotting disorders, stroke, or myocardial infarction.
  • Current or past diagnosis of hormone‑dependent cancers such as breast or endometrial cancer.
  • Uncontrolled hypertension or significant cardiovascular disease.
  • Smoking in women over 35 years of age.
  • Liver disease that impairs hormone metabolism.
  • Pregnancy or suspected pregnancy.
  • Known allergy to drospirenone, ethinylestradiol, or lactose.

Avoid Interactions

Hastina 21+7 can interact with other medicines, affecting its effectiveness or safety.

Avoid

  • Anticoagulants such as warfarin, which may have reduced efficacy.
  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin) that lower hormone levels.
  • Certain antibiotics like rifampin that increase hormone metabolism.
  • St. John’s wort, a herbal inducer of hepatic enzymes.
  • HIV protease inhibitors that may increase estrogen levels.

Use with caution

  • Antifungal agents (e.g., ketoconazole) that can raise hormone concentrations.
  • Selective serotonin reuptake inhibitors (SSRIs) that may slightly increase clot risk.
  • Diuretics that may affect potassium balance when combined with drospirenone.

Frequently Asked Questions

Hastina 21+7 works by suppressing the release of luteinizing hormone (LH) and follicle‑stimulating hormone (FSH), which prevents ovulation, and it also induces changes in cervical mucus and the endometrium that reduce the chance of fertilisation.

The tablet is taken once daily at the same time each day for 21 consecutive days, followed by a 7‑day hormone‑free interval during which withdrawal bleeding usually occurs.

Yes, the first tablet can be started on the first day of menstrual bleeding; however, a backup contraceptive method is recommended for the first 7 days of active tablets.

Lactose anhydrous is present only as an inactive filler in small amounts; most lactose‑intolerant individuals can use the product without problems, but those with severe sensitivity should consult a healthcare professional.

Common side effects include nausea, mild headache, breast tenderness, and spotting or breakthrough bleeding, especially during the first few cycles.

The tablet should be discontinued if a serious adverse event occurs, such as signs of blood clot, severe allergic reaction, or if pregnancy is confirmed.

Smoking, particularly in women over 35 years of age, raises the risk of cardiovascular events and blood clots when using combined oral contraceptives like Hastina 21+7.

Most short‑course antibiotics do not affect contraceptive efficacy, but enzyme‑inducing antibiotics such as rifampin can reduce hormone levels and should be avoided or supplemented with additional contraception.

Weight changes are not a consistent effect of combined oral contraceptives; any perceived weight gain is usually due to fluid retention and typically resolves over time.

Hastina 21+7 contains drospirenone, a progestogen with anti‑aldosterone activity, which may lead to less water retention compared with some other progestins.

Drospirenone‑containing contraceptives can improve acne in some patients, but Hastina 21+7 is primarily approved for pregnancy prevention; acne treatment should be discussed with a clinician.

If a tablet is missed, it should be taken as soon as remembered; if more than 12 hours have passed, use a backup method for the next 7 days and continue the regular schedule.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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