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Index of reports
> All cases (46)
Below is the selection of adverse event reports related to Motrin (Ibuprofen) that includes all cases.
Reports 1 - 25 of 46 Next >>
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-30
Patient: female
Adverse reactions / side effects: Myalgia, Arthralgia, ECG Signs of Myocardial Ischaemia, Chest Expansion Decreased, Chest Pain
Suspect drug(s):
Chantix
Indication: Smoking Cessation Therapy
Motrin
Indication: Chest Pain
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-17
Patient: female, weighing 64.6 kg (142.2 pounds)
Adverse reactions / side effects: Drug Ineffective, Chest Pain, Electrocardiogram Abnormal
Suspect drug(s):
Motrin
Indication: Chest Pain
Chantix
Indication: Smoking Cessation Therapy
Other drugs received by patient: Darvocet
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 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 9 month old male receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-07-09
Patient: 9 month old male, weighing 8.4 kg (18.5 pounds)
Adverse reactions / side effects: Wheezing, Rash
Suspect drug(s):
Motrin
Dosage: 50 mg, 1 in 6 hour, oral
Administration route: Oral
Indication: Pyrexia
Start date: 2007-04-16
End date: 2007-04-17
Motrin
Dosage: 50 mg, 1 in 6 hour, oral
Administration route: Oral
Indication: Rash
Start date: 2007-04-16
End date: 2007-04-17
Other drugs received by patient: Acetaminophen
Adverse event in 15 month old female receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-07-09
Patient: 15 month old female, weighing 8.6 kg (19.0 pounds)
Adverse reactions / side effects: Wheezing
Suspect drug(s):
Motrin
Dosage: 75 mg, 2 in 1 day
Indication: Pyrexia
Start date: 2007-03-21
Motrin
Dosage: 75 mg, 2 in 1 day
Indication: Pyrexia
Start date: 2007-03-22
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 7 month old female receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-07-09
Patient: 7 month old female, weighing 9.2 kg (20.2 pounds)
Adverse reactions / side effects: Hypersensitivity
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
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 64 year old female receiving Motrin (Ibuprofen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-23
Patient: 64 year old female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Blood Pressure Diastolic Increased
Suspect drug(s):
Motrin (Ibuprofen)
Adverse event in receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-05-21
Patient:
Adverse reactions / side effects: Drug Interaction, Impaired Gastric Emptying
Suspect drug(s):
Januvia
Dosage: po
Administration route: Oral
Motrin
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a consumer/non-health professional from United States on 2007-05-17
Patient: female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Incision Site Pain, Chest Discomfort
Suspect drug(s):
Motrin
Indication: Procedural Pain
Chantix
Indication: Smoking Cessation Therapy
Other drugs received by patient: Acetaminophen and Hydrocodone Bitartrate
Adverse event in female receiving Motrin (Ibuprofen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-10
Patient: female, weighing 125.6 kg (276.4 pounds)
Adverse reactions / side effects: Pruritus, Nausea
Suspect drug(s):
Motrin
Dosage: 800 mg 1 three times a day per orem
Indication: Arthritis
Start date: 1995-01-01
Motrin
Dosage: 800 mg 1 three times a day per orem
Indication: Fibromyalgia
Start date: 1995-01-01
Motrin
Dosage: 800 mg 1 three times a day per orem
Indication: Neuropathy Peripheral
Start date: 1995-01-01
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 female receiving Motrin (Ibuprofen)
Reported by a physician from United States on 2007-04-26
Patient: female, weighing 56.7 kg (124.7 pounds)
Adverse reactions / side effects: Respiratory Disorder, Angina Pectoris, Palpitations, Extrasystoles, Somatisation Disorder, Ulcer Haemorrhage, Epistaxis
Suspect drug(s):
Celebrex
Indication: Bone Pain
Start date: 2006-02-01
End date: 2006-04-11
Celebrex
Indication: Swelling
Celebrex
Indication: Back Disorder
Motrin
Dosage: freq:unknown
Indication: Bone Pain
Motrin
Indication: Swelling
Motrin
Indication: Back Disorder
Other drugs received by patient: Vicodin; Tylenol; Zyrtec
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 consumer/non-health professional from United States on 2007-04-16
Patient: female
Adverse reactions / side effects: Haematochezia, Blood Urine Present, Rash Papular, Carotid Artery Occlusion, Gastric Haemorrhage
Suspect drug(s):
Motrin
Administration route: Oral
Indication: Arthralgia
Plavix
Administration route: Oral
Indication: Cerebrovascular Accident
Other drugs received by patient: Ultram; Darvocet; Ezetimibe
Adverse event in 4 year old male receiving Motrin (Ibuprofen)
Reported by a individual with unspecified qualification from United States on 2007-04-13
Patient: 4 year old male, weighing 18.1 kg (39.9 pounds)
Adverse reactions / side effects: Gait Disturbance
Suspect drug(s):
Motrin (Ibuprofen)
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