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Motrin (Ibuprofen) - Adverse Event Reports - All Cases - Drug Exposure During Pregnancy

 



Index of reports > All cases (46) > Cases with Drug Exposure During Pregnancy (6)

Below is the selection of adverse event reports related to Motrin (Ibuprofen) that includes all cases 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 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



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

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