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Index of reports
> Cases resulting in a serious event (43)
> Cases with Drug Exposure During Pregnancy (6)
Below is the selection of adverse event reports related to Motrin (Ibuprofen) that includes cases resulting in a serious event where reactions include drug exposure during pregnancy.
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-07-17
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Spontaneous
Suspect drug(s):
Motrin (Ibuprofen)
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-07-02
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Pregnancy Induced Hypertension, Premature Labour
Adverse event resulted in: hospitalization
Suspect drug(s):
Motrin
Administration route: Oral
Indication: Premedication
Rebif
Indication: Multiple Sclerosis
Zomig
Administration route: Oral
Indication: Migraine
Adverse event in male receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-07-02
Patient: male, weighing 2.4 kg (5.3 pounds)
Adverse reactions / side effects: Asthma, Dysphagia, Premature Baby, Drug Exposure During Pregnancy, Aspiration, Nystagmus, Jaundice Neonatal
Adverse event resulted in: hospitalization
Suspect drug(s):
Motrin
Indication: Drug Exposure During Pregnancy
Rebif
Indication: Drug Exposure During Pregnancy
Zomig
Indication: Drug Exposure During Pregnancy
Adverse event in 31 year old female receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-06-27
Patient: 31 year old female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Pregnancy Induced Hypertension, Premature Labour
Suspect drug(s):
Zomig
Administration route: Oral
Indication: Migraine
Start date: 2005-08-01
End date: 2005-08-01
Rebif
Indication: Multiple Sclerosis
Start date: 2005-06-22
End date: 2005-08-24
Motrin
Indication: Premedication
Start date: 2005-06-01
End date: 2005-08-01
Adverse event in 31 year old female receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-06-22
Patient: 31 year old female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Pregnancy Induced Hypertension, Premature Labour
Suspect drug(s):
Rebif
Dosage: 44 mcg, 3 in 1 weeks, subcutaneous
Indication: Multiple Sclerosis
Start date: 2005-06-22
End date: 2005-08-24
Zomig
Dosage: 2.5 mg, as required, oral
Administration route: Oral
End date: 2005-08-01
Motrin
Dosage: 800 mg, as required, oral
Administration route: Oral
Start date: 2005-06-01
End date: 2005-08-01
Adverse event in male receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-06-22
Patient: male, weighing 2.4 kg (5.3 pounds)
Adverse reactions / side effects: Asthma, Dysphagia, Drug Exposure During Pregnancy, Neonatal Aspiration, Congenital Nystagmus, Jaundice Neonatal
Adverse event resulted in: hospitalization
Suspect drug(s):
Rebif
Dosage: 44 mcg, 3 in 1 weeks, subcutaneous
Indication: Multiple Sclerosis
Start date: 2005-06-22
End date: 2005-08-01
Zomig
Dosage: 2.5 mg, as required, oral
Administration route: Oral
End date: 2005-08-01
Motrin
Dosage: 800 mg, as required, oral
Administration route: Oral
Start date: 2005-06-01
End date: 2005-08-01
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