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Index of reports
> Cases resulting in life threatening events (3)
Below is the selection of adverse event reports related to Motrin (Ibuprofen) that includes cases resulting in life threatening events.
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-02-06
Patient: female, weighing 68.9 kg (151.7 pounds)
Adverse reactions / side effects: Vomiting, Cerebrovascular Accident, Hyperhidrosis, Dysphemia, Anxiety, Dysstasia, Malaise, Diarrhoea, Injury, Asthenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Motrin (Ibuprofen)
Adverse event in 40 year old female receiving Motrin (Ibuprofen)
Reported by a pharmacist from United States on 2007-02-01
Patient: 40 year old female, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Vomiting, Medication Error, Nausea, Incorrect Dose Administered, Abdominal Pain Upper, Haematemesis
Adverse event resulted in: life threatening event
Suspect drug(s):
Motrin
Indication: Toothache
Start date: 2007-01-12
End date: 2007-01-26
Tylenol
Indication: Toothache
Start date: 2007-01-12
End date: 2007-01-26
Adverse event in 73 year old female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-01-19
Patient: 73 year old female
Adverse reactions / side effects: Gastrointestinal Haemorrhage, Pain, Dyspnoea Exertional, Haematocrit Decreased, Fatigue, Iron Deficiency Anaemia, Pulmonary Oedema, Muscle Spasms, Hiatus Hernia, Stomach Discomfort, Occult Blood Positive, Haemoglobin Decreased, Syncope, Diverticulum, Ventricular Tachycardia, Suicide Attempt, Asthenia, Depressed Mood
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Aleve
Dosage: total daily dose: 880 mg unit dose: 220 mg
Administration route: Oral
Indication: Arthralgia
Motrin
Dosage: total daily dose: 2400 mg unit dose: 800 mg
Indication: Osteoarthritis
Naprosyn
Indication: Osteoarthritis
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