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Review Microgynon Safety Reports submitted to FDA

Total Microgynon reports: 4.
Microgynon FDA safety alerts: No.
   Reported hospitalizations: 2.
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FDA Reported Microgynon Side Effects: surgery, liver disorder, gastrointestinal carcinoma, aspartate aminotransferase increased, alanine aminotransferase increased.
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Microgynon Side Effects Report #5675064-8
Health Professional from UNITED KINGDOM reported MICROGYNON problem on Mar 11, 2008. Female patient, 31 years of age, was diagnosed with contraception, insomnia, depression, osteopenia, fatigue and was treated with MICROGYNON. After drug was administered, patient experienced the following problems/side effects: erythema, lupus-like syndrome, musculoskeletal stiffness, pain, rash, rash erythematous, skin lesion, swelling. MICROGYNON dosage: unknown. During the same period patient was treated with NIFEDIPINE, AMITRIPTYLINE, CALCICHEW, PROVIGIL. Patient recovered.

Microgynon Side Effects Report #5687680-8
MICROGYNON problem was reported by a Health Professional from UNITED KINGDOM on Mar 19, 2008. Female patient, 31 years of age, was diagnosed with contraception, insomnia, depression, osteopenia, fatigue and was treated with MICROGYNON. After drug was administered, patient experienced the following problems/side effects: erythema, lupus-like syndrome, musculoskeletal stiffness, pain, rash, rash erythematous, skin lesion, swelling. MICROGYNON dosage: unknown. During the same period patient was treated with NIFEDIPINE, AMITRIPTYLINE, CALCICHEW, PROVIGIL. Patient recovered.

Microgynon Side Effects Report #5599798-9
Consumer or non-health professional from UNITED KINGDOM reported MICROGYNON problem on Dec 28, 2007. Female patient, 21 years of age, was treated with MICROGYNON. After drug was administered, patient experienced the following problems/side effects: eye disorder, eye infection, thrombosis, toxoplasmosis. MICROGYNON dosage: unknown. Patient was hospitalized. Patient recovered.

Microgynon Side Effects Report #5572317-9
MICROGYNON problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 29, 2007. Female patient, 21 years of age, was treated with MICROGYNON. After drug was administered, patient experienced the following problems/side effects: eye disorder, eye infection, thrombosis, toxoplasmosis. MICROGYNON dosage: unknown. Patient was hospitalized. Patient recovered.


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erythema, lupus-like syndrome, musculoskeletal stiffness, pain, rash, rash erythematous, skin lesion, swelling, , was diagnosed with contraception, insomnia, depression, osteopenia, fatigue and was diagnosed with contraception, insomnia, depression, osteopenia, fatigue and