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Index of reports
> Cases resulting in hospitalization (18)
Below is the selection of adverse event reports related to Motrin (Ibuprofen) that includes cases resulting in hospitalization.
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: female, weighing 77.3 kg (170.0 pounds)
Adverse reactions / side effects: Nerve Injury, Drug Ineffective, Drug Interaction, Pelvic Pain, Somnolence, Suicidal Ideation, Thinking Abnormal, Fatigue, Chest Pain, Clumsiness, Hysterectomy, Panic Attack, Loss of Employment, Incision Site Infection, Limb Injury, Vision Blurred, Gait Disturbance, Depressed Mood
Adverse event resulted in: hospitalization
Suspect drug(s):
Gabapentin
Indication: Pelvic Pain
Gabapentin
Indication: Nerve Injury
Motrin
Indication: Pelvic Pain
Other drugs received by patient possibly interacting with the suspect drug:
Xanax
Indication: Psychomotor Hyperactivity
Xanax
Indication: Depression
Hismanal
Other drugs received by patient: Lopressor; Mevacor; Claritin; Dyazide; Aspirin
Adverse event in 14 month old female receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-07-09
Patient: 14 month old female, weighing 12.7 kg (27.9 pounds)
Adverse reactions / side effects: Skin Discolouration, Pain, Oedema Peripheral, Rash
Adverse event resulted in: hospitalization
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 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 57 year old female receiving Motrin (Ibuprofen)
Reported by a lawyer from United States on 2007-06-21
Patient: 57 year old female
Adverse reactions / side effects: Respiratory Failure, Pneumonia Streptococcal, Mitral Valve Incompetence, Troponin Increased, Sputum Culture Positive, Multiple Drug Overdose, Tricuspid Valve Incompetence
Adverse event resulted in: hospitalization
Suspect drug(s):
Buspar
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Motrin
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Ultram
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Soma
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Lorazepam
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Other drugs received by patient: Claritin; Neurontin; Celexa; Phenazopyridine HCL TAB; Dalmane; Potassium Chloride
Adverse event in 57 year old female receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-05-25
Patient: 57 year old female
Adverse reactions / side effects: Pneumonia Aspiration, Unresponsive TO Stimuli, Tricuspid Valve Incompetence, Somnolence, Foaming AT Mouth, Cyanosis, Sputum Culture Positive, Multiple Drug Overdose, Apnoea, Blood Glucose Increased, Blood Urea Increased, Blood Pressure Systolic Increased, Haemophilus Infection, Blood Chloride Increased, Troponin Increased, Streptococcal Infection, Aggression, Convulsion, Heart Rate Increased, Mitral Valve Incompetence
Adverse event resulted in: hospitalization
Suspect drug(s):
Soma (Carisoprodol, Usp) 350mg
Dosage: 87 tablets (350 mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Motrin
Dosage: 71 tablets (800 mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Buspar
Dosage: 33 tablets (5 mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Ultram
Dosage: 100 tablets, oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Lorazepam
Dosage: 28 tablets (30mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Other drugs received by patient: Claritin; Neurontin; Celexa; Phenazopyridine HCL TAB; Dalmane; Potassium Chloride
Adverse event in 28 year old male receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-05-07
Patient: 28 year old male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Renal Disorder, Drug Ineffective, Dialysis, Blood Pressure Inadequately Controlled, Appendicectomy, Pharmaceutical Product Complaint, Hypertension, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Adalat
Dosage: total daily dose: 90 mg
Administration route: Oral
Indication: Hypertension
Motrin
Dosage: total daily dose: 1800 mg
Administration route: Oral
Indication: Swelling
Start date: 1995-03-29
End date: 1995-04-16
Motrin
Dosage: total daily dose: 1800 mg
Administration route: Oral
Start date: 1995-04-24
End date: 1995-05-23
Adverse event in 60 year old female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-04-24
Patient: 60 year old female, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Haematemesis
Adverse event resulted in: hospitalization
Suspect drug(s):
Clonazepam
Indication: Drug USE FOR Unknown Indication
Start date: 2006-11-22
PEG-Interferon Alfa 2A (RO 25-8310)
Start date: 2006-01-19
End date: 2006-12-14
Ribavirin
Administration route: Oral
Start date: 2006-01-19
End date: 2006-12-19
Lisinopril
Indication: Drug USE FOR Unknown Indication
Start date: 2005-10-27
Zinc
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-01
Hydrochlorothiazide
Indication: Drug USE FOR Unknown Indication
Start date: 2006-11-11
Motrin
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-19
Propranolol
Indication: Drug USE FOR Unknown Indication
Calcium
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Sertraline
Adverse event in 60 year old female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-04-16
Patient: 60 year old female, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Haematemesis
Adverse event resulted in: hospitalization
Suspect drug(s):
Clonazepam
Indication: Drug USE FOR Unknown Indication
Start date: 2006-11-22
PEG-Interferon Alfa 2A (RO 25-8310)
Start date: 2006-01-19
End date: 2006-12-19
Ribavirin
Administration route: Oral
Start date: 2006-01-19
End date: 2006-12-19
Lisinopril
Indication: Drug USE FOR Unknown Indication
Start date: 2005-10-27
Zinc
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-01
Hydrochlorothiazide
Indication: Drug USE FOR Unknown Indication
Start date: 2006-11-11
Motrin
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-19
Propranolol
Indication: Drug USE FOR Unknown Indication
Calcium
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Sertraline
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-04-06
Patient: female
Adverse reactions / side effects: Respiratory Failure, Multiple Drug Overdose
Adverse event resulted in: hospitalization
Suspect drug(s):
Motrin
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Ultram
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Buspar
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Soma
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Lorazepam
Dosage: 30 mg, 28-30 total
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Flurazepam; Claritin; Neurontin; Celexa; Potassium Chloride; Acetaminophen and Hydrocodone Bitartrate
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a lawyer from United States on 2007-04-03
Patient: female
Adverse reactions / side effects: Drug Ineffective, Respiratory Failure, Suicide Attempt, Multiple Drug Overdose
Adverse event resulted in: hospitalization
Suspect drug(s):
Neurontin
Administration route: Oral
Indication: Depression
Neurontin
Indication: Nerve Injury
Soma
Buspar
Motrin
Lorazepam
Tramadol HCL
Adverse event in 28 year old male receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-03-30
Patient: 28 year old male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Renal Disorder, Blood Pressure Inadequately Controlled, Appendicectomy, Hypertension, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Adalat
Dosage: total daily dose: 90 mg
Administration route: Oral
Indication: Hypertension
Motrin
Dosage: total daily dose: 1800 mg
Administration route: Oral
Indication: Swelling
Start date: 1995-03-29
End date: 1995-04-16
Motrin
Dosage: total daily dose: 1800 mg
Administration route: Oral
Start date: 1995-04-24
End date: 1995-05-23
Adverse event in 28 year old male receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-02-22
Patient: 28 year old male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Renal Disorder, Blood Pressure Inadequately Controlled, Appendicectomy, Hypertension, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Adalat
Dosage: total daily dose: 90 mg
Administration route: Oral
Indication: Hypertension
Motrin
Dosage: total daily dose: 1800 mg
Administration route: Oral
Indication: Swelling
Start date: 1995-03-29
End date: 1995-04-16
Motrin
Dosage: total daily dose: 1800 mg
Administration route: Oral
Start date: 1995-04-24
End date: 1995-05-23
Adverse event in male receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-02-02
Patient: male, weighing 79.4 kg (174.6 pounds)
Adverse reactions / side effects: Renal Failure, Appendicectomy, Hypertension
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Motrin
Motrin
Indication: Back Injury
Adalat
Indication: Hypertension
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-01-26
Patient: female
Adverse reactions / side effects: Fluid Overload, Gastrointestinal Haemorrhage, Diverticulum, Hiatus Hernia, Iron Deficiency Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Motrin
Indication: Osteoarthritis
Aleve
Indication: Osteoarthritis
Naprosyn
Administration route: Oral
Indication: Osteoarthritis
Adverse event in 49 year old male receiving Motrin (Ibuprofen)
Reported by a pharmacist from United States on 2007-01-22
Patient: 49 year old male, weighing 105.0 kg (231.0 pounds)
Adverse reactions / side effects: Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Salsalate 750mg
Dosage: 750mg q8 h prn po
Administration route: Oral
Indication: Back Pain
Start date: 2006-08-21
Motrin
Dosage: 800mg prn po
Administration route: Oral
Indication: Pain
ASA 81 MG Daily PO
Dosage: 81mg daily po
Administration route: Oral
Start date: 2006-06-04
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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