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Index of reports
> Cases with Product Quality Issue ()
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Motrin (Ibuprofen) where reactions include product quality issue. 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 consumer/non-health professional from United States on 2012-07-20
Patient: female, weighing 68.0 kg (149.7 pounds)
Reactions: Product Quality Issue, Chest Discomfort, Drug Ineffective, Chest Pain
Drug(s) suspected as cause:
Motrin
Dosage: unk
Start date: 2012-06-01
Protonix
Dosage: 40 mg, 1x/day
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2007-01-01
Protonix
Dosage: 40 mg, daily
Administration route: Oral
Start date: 2012-06-01
End date: 2012-06-01
Other drugs received by patient: Lithium; Fuzeon; Thorazine; Lamictal; Synthroid; Lorazepam; Combivent; Advair Diskus 100 / 50
Possible Motrin side effects in
Reported by a health professional (non-physician/pharmacist) from United States on 2012-06-28
Patient: , weighing 19.8 kg (43.6 pounds)
Reactions: Product Quality Issue, Joint Swelling, Urticaria, Ear Infection, Erythema
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Children's Benadryl Allergy
Administration route: Oral
Children's Benadryl Allergy
Dosage: daily dose text: unknown
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Children's Motrin
Dosage: daily dose text: unknown
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Children's Tylenol Suspension
Dosage: daily dose text: unknown
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Motrin
Dosage: daily dose text: unknown
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Possible Motrin side effects in female
Reported by a consumer/non-health professional from United States on 2012-03-14
Patient: female, weighing 66.7 kg (146.7 pounds)
Reactions: Product Quality Issue, Dysphagia, Gastritis Erosive, Change of Bowel Habit, Constipation, Therapeutic Response Decreased, Dysphonia, Gastrointestinal Oedema, Small Intestinal Stenosis, Sinusitis
Drug(s) suspected as cause:
Motrin
Indication: Product Used FOR Unknown Indication
Remicade
Dosage: dose: 4 vials of 100 mg each
Indication: Crohn's Disease
Start date: 2009-01-01
Zantac
Indication: Gastritis Erosive
Start date: 2011-01-01
Other drugs received by patient: Prilosec
Possible Motrin side effects in male
Reported by a consumer/non-health professional from United States on 2012-01-16
Patient: male
Reactions: Product Quality Issue, Drug Ineffective, Anaphylactic Reaction, Pyrexia, Thirst
Drug(s) suspected as cause:
Children's Benadryl Allergy
Dosage: daily dose text: unknown
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Children's Benadryl Allergy
Administration route: Oral
Motrin
Dosage: daily dose text: unknown
Administration route: Oral
Indication: Product Used FOR Unknown Indication
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