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Index of reports
> Death (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Motrin (Ibuprofen) death. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Motrin side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-03-28
Patient: female, weighing 48.0 kg (105.6 pounds)
Reactions: Renal Failure, Drug Interaction, Hepatic Failure
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Acetaminophen
Dosage: 1000-2000 mg per week on average
Indication: Headache
Montelukast
Start date: 2003-07-03
Motrin
Start date: 2003-07-05
Zyrtec
Start date: 2003-07-03
Acetaminophen
Other drugs received by patient possibly interacting with the suspect drug:
Extra Strength Tylenol PM
Administration route: Oral
Indication: Insomnia
Start date: 2004-09-03
Levothyroxine Sodium
Dosage: day 12 of cycle 8
Indication: Hypothyroidism
Start date: 2005-05-31
Levothyroxine Sodium
Dosage: on day 28 of cycle 8
Sunitinib Malate
Dosage: repeating 6 wk cycles of 4 wk on 50 mg/day followed by 2 wks off treatment
Administration route: Oral
Indication: Gastrointestinal Stromal Tumour
Start date: 2004-07-16
End date: 2005-07-02
Levothyroxine Sodium
Dosage: after 1 week of starting the 50 ug
Other drugs received by patient: Megace; Prevacid; Eucerin; Albuterol; Zantac
Possible Motrin side effects in female
Reported by a consumer/non-health professional from United States on 2012-02-28
Patient: female
Reactions: Gastric Ulcer
Adverse event resulted in: death
Drug(s) suspected as cause:
Motrin
Nexium
Administration route: Oral
Indication: Dyspepsia
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