Femipil 0.03 mg+0.15 mg+75 mg (Tablet)
Medicine Details
Category | Details |
---|---|
Generic | Ethinyl estradiol levonorgestrel ferrous fumarate |
Company | Beximco pharmaceuticals ltd |
Indications
- Inhibit Ovulation
- Inhibit sperm to enter into the uterus by condensing uterine mucus
- Inhibit fertilized egg to accept by uterus by protecting the growth of membrane inside the uterus
- Reduces the movement of sperm by minimizing normal movement of fallopian tube
- Suitable for women aged between 15-69 years (except smoker and who use tobacco regularly)
- Temporary contraceptive method for women
- Anemia treatment due to excessive blood loss during menstruation
- Management of irregular menstruation cycle
- Suitable for breastfeeding mothers (if child age is more than 6 months)
Composition
Each White (Hormone) Tablet contains Ethinylestradiol USP 0.03 mg & Levonorgestrel USP 0.15 mg. Each Brown color (Iron) tablet contains Ferrous Fumarate BP 75 mg.
Pharmacology
Contains Levonorgestrel and Ethinyl Estradiol. Suppresses ovulation. May include cervical mucus changes inhibiting sperm penetration and endometrial changes reducing likelihood of implantation.
Dosage & Administration
Start taking tablet from the first day of menstruation. Take one tablet same time each day. Start with white tablet for 3 weeks, then brown tablet for 7 days. If menstruation starts while taking brown tablet, continue the medication.
Interaction
Enzyme inducers may decrease effectiveness. Avoid caffeine, dairy foods, phytic acid containing food while taking the drug.
Contraindications
Known hypersensitivity to any of the components of this product.
Side Effects
- Headache
- Nausea
- Mood changes including depression
- Vaginal infections
- Irregular vaginal bleeding
- Pain and discomfort
- Liver tumors
- Jaundice
- High blood pressure
- Gallbladder problem
Pregnancy & Lactation
- Contraindicated in pregnancy
- Discontinue if pregnancy occurs
- Reduce milk production in breastfeeding females
Precautions & Warnings
- Stop if a thrombotic disorder occurs
- Stop at least 4 weeks before through 2 weeks after major surgery
- Discontinue if jaundice occurs
- Monitor blood pressure and stop if it rises significantly
- Monitor prediabetic and diabetic women
- Evaluate significant change in headaches and discontinue if indicated
- Evaluate irregular bleeding or amenorrhea
Use in Special Populations
Safety and efficacy established in women of reproductive age. Efficacy expected to be the same in post-pubertal adolescents under the age of 18 years.
Overdose Effects
No reports of serious illness effects. Over dosage may cause withdrawal bleeding in females and nausea.
Therapeutic Class
Oral Contraceptive preparations
Storage Conditions
Store below 30°C, protected from light and moisture. Keep all medicines out of reach of children.
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