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Bravelle (Urofollitropin) - Side Effect Reports to FDA


This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Bravelle (Urofollitropin) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (1)

Reports by Reaction Type

Maternal Exposure During Pregnancy (1)Abortion Spontaneous (1)

Possible Bravelle side effects in female

Reported by a consumer/non-health professional from United States on 2011-10-19

Patient: female, weighing 79.4 kg (174.6 pounds)

Reactions: Maternal Exposure During Pregnancy, Abortion Spontaneous

Drug(s) suspected as cause:
    Dosage: (150 -0225 iu everyday (qd))
    Indication: in Vitro Fertilisation
    Start date: 2009-11-01
    End date: 2009-11-23

    Indication: in Vitro Fertilisation
    Start date: 2009-11-01
    End date: 2009-11-23

Other drugs received by patient: Prenatal Vitamins / 01549301 /; Progesterone

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