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Index of reports
> Cases resulting in hospitalization (20)
Below is the selection of adverse event reports related to Naprosyn (Naproxen) that includes cases resulting in hospitalization.
Adverse event in 52 year old male receiving Naprosyn (Naproxen)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-17
Patient: 52 year old male
Adverse reactions / side effects: Dyspnoea, Eosinophilic Pneumonia, Arthralgia, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn
Administration route: Oral
Indication: Tooth Abscess
Start date: 2007-01-29
End date: 2007-02-03
Omeprazole
Administration route: Oral
Start date: 2007-01-29
End date: 2007-02-03
Rodogyl
Administration route: Oral
Indication: Tooth Abscess
Start date: 2007-01-29
End date: 2007-02-05
Adverse event in 52 year old male receiving Naprosyn (Naproxen)
Reported by a individual with unspecified qualification on 2007-10-17
Patient: 52 year old male
Adverse reactions / side effects: Dyspnoea, Eosinophilic Pneumonia, Arthralgia, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn
Administration route: Oral
Start date: 2007-01-29
End date: 2007-02-03
Omeprazole
Administration route: Oral
Start date: 2007-01-29
End date: 2007-02-03
Rodogyl
Administration route: Oral
Start date: 2007-01-29
End date: 2007-02-05
Adverse event in male receiving Naprosyn (Naproxen)
Reported by a consumer/non-health professional from United States on 2007-10-10
Patient: male
Adverse reactions / side effects: Contusion, Dyspnoea, Restlessness, Abnormal Behaviour, Disorientation, Fall, Pericardial Effusion, Hydrothorax, Renal Impairment, Cardiac Failure Congestive
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ambien
Dosage: dose: unk
Indication: Insomnia
Start date: 2007-08-27
Colchicine
Dosage: dose: unk
End date: 2007-08-01
Furosemide
Dosage: dose: unk
End date: 2007-08-01
Naprosyn
Dosage: dose: unk
End date: 2007-08-01
Plavix
Dosage: dose: unk
Indication: Cardiac Failure Congestive
Adverse event in male receiving Naprosyn (Naproxen)
Reported by a consumer/non-health professional from United States on 2007-10-09
Patient: male
Adverse reactions / side effects: Renal Disorder, Dyspnoea, Contusion, Abnormal Behaviour, Disorientation, Fall, Pericardial Effusion, Pulmonary Oedema, Cardiac Failure Congestive
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ambien
Dosage: unk
Indication: Sleep Disorder
Start date: 2007-08-27
Colchicine
Dosage: unk
Indication: Drug USE FOR Unknown Indication
End date: 2007-08-01
Furosemide
Dosage: unk
Indication: Drug USE FOR Unknown Indication
End date: 2007-08-01
Naprosyn
Dosage: unk
Indication: Drug USE FOR Unknown Indication
End date: 2007-08-01
Plavix
Dosage: unk
Administration route: Oral
Adverse event in 46 year old male receiving Naprosyn (Naproxen)
Reported by a health professional (non-physician/pharmacist) from NEW Zealand on 2007-06-28
Patient: 46 year old male
Adverse reactions / side effects: Metabolic Acidosis, Intentional Overdose, Hypotension
Adverse event resulted in: hospitalization
Suspect drug(s):
Allopurinol
Indication: Intentional Overdose
Start date: 2007-01-01
Allopurinol
Indication: Suicide Attempt
Start date: 2007-01-01
Colchicum JTL LIQ
Dosage: oral
Administration route: Oral
Indication: Intentional Overdose
Start date: 2007-01-01
Colchicum JTL LIQ
Dosage: oral
Administration route: Oral
Indication: Suicide Attempt
Start date: 2007-01-01
Naprosyn
Indication: Intentional Overdose
Naprosyn
Indication: Suicide Attempt
Adverse event in 72 year old male receiving Naprosyn (Naproxen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-22
Patient: 72 year old male
Adverse reactions / side effects: Dyspnoea, Staphylococcal Infection, Drug Interaction, Skin Burning Sensation, Rash, Eye Infection, Erythema, Shock
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn
Dosage: 500 mg bid po
Administration route: Oral
Indication: Pain
Start date: 2006-10-15
Niaspan
Start date: 2007-03-01
End date: 2007-04-01
Plavix
Indication: Stent Placement
Adverse event in 72 year old male receiving Naprosyn (Naproxen)
Reported by a consumer/non-health professional from United States on 2007-06-01
Patient: 72 year old male
Adverse reactions / side effects: Eye Infection Staphylococcal, Skin Ulcer, Staphylococcal Infection, Drug Interaction, Skin Reaction
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn
Administration route: Oral
Indication: Cyst
Start date: 2006-10-01
Niaspan
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient possibly interacting with the suspect drug:
Plavix
Indication: Drug USE FOR Unknown Indication
Adverse event in 72 year old male receiving Naprosyn (Naproxen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-30
Patient: 72 year old male
Adverse reactions / side effects: Burning Sensation, Localised Infection, Dyspnoea, Staphylococcal Infection, Drug Interaction, Rash, Eye Infection, Erythema, Shock
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn
Dosage: 500 mg bid po
Administration route: Oral
Indication: Pain
Start date: 2006-10-15
Niaspan
Plavix
Indication: Stent Placement
Adverse event in female receiving Naprosyn (Naproxen)
Reported by a physician from Hungary on 2007-05-25
Patient: female
Adverse reactions / side effects: Venous Thrombosis Limb
Adverse event resulted in: hospitalization
Suspect drug(s):
Famotidine
Naprosyn
Administration route: Oral
Panitumumab
Indication: Colorectal Cancer
Start date: 2007-03-01
End date: 2007-03-01
Perindopril
Tramadol HCL
Adverse event in female receiving Naprosyn (Naproxen)
Reported by a physician from Hungary on 2007-05-18
Patient: female
Adverse reactions / side effects: Venous Thrombosis Limb
Adverse event resulted in: hospitalization
Suspect drug(s):
Famotidine
Naprosyn
Administration route: Oral
Panitumumab
Indication: Colorectal Cancer
Start date: 2007-03-01
End date: 2007-03-01
Perindopril
Tramadol HCL
Adverse event in 63 year old male receiving Naprosyn (Naproxen)
Reported by a pharmacist from United States on 2007-05-14
Patient: 63 year old male, weighing 84.4 kg (185.6 pounds)
Adverse reactions / side effects: Gastrointestinal Ulcer, Diverticulum, Gastrointestinal Haemorrhage
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn (Naproxen)
Adverse event in 72 year old male receiving Naprosyn (Naproxen)
Reported by a consumer/non-health professional from United States on 2007-05-01
Patient: 72 year old male
Adverse reactions / side effects: Eye Infection Staphylococcal, Staphylococcal Infection, Drug Interaction, Skin Reaction
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn
Administration route: Oral
Indication: Cyst
Start date: 2006-10-01
Niaspan
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient possibly interacting with the suspect drug:
Plavix
Indication: Drug USE FOR Unknown Indication
Adverse event in 63 year old male receiving Naprosyn (Naproxen)
Reported by a pharmacist from United States on 2007-04-13
Patient: 63 year old male, weighing 84.4 kg (185.6 pounds)
Adverse reactions / side effects: Barrett's Oesophagus, Gastrointestinal Haemorrhage, Heart Rate Increased, Diverticulitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn (Naproxen)
Adverse event in 68 year old receiving Naprosyn (Naproxen)
Reported by a pharmacist from United States on 2007-04-11
Patient: 68 year old
Adverse reactions / side effects: Haemoglobin Decreased, Gastrointestinal Haemorrhage, Haematocrit Decreased, Malaise, Melaena
Adverse event resulted in: hospitalization
Suspect drug(s):
Aspirin
Dosage: 81 mg daily po
Administration route: Oral
Indication: Coronary Artery Disease
Indocin
Dosage: previous rx for flare po
Administration route: Oral
Indication: Gout
Naprosyn
Dosage: otc use 3x per week po
Administration route: Oral
Indication: Pain
Other drugs received by patient: Colchicine; Ezetimibe; Diltiazem; Pyridoxine HCL; Hydralazine HCL; Hydrochlorothiazide
Adverse event in 46 year old male receiving Naprosyn (Naproxen)
Reported by a physician from NEW Zealand on 2007-04-10
Patient: 46 year old male
Adverse reactions / side effects: Metabolic Acidosis, Hypotension, Multiple Drug Overdose Intentional
Adverse event resulted in: hospitalization
Suspect drug(s):
Allopurinol
Colchicine(colchicine)
Naprosyn
Adverse event in 15 year old female receiving Naprosyn (Naproxen)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-04
Patient: 15 year old female
Adverse reactions / side effects: Tachycardia, Anaemia, Dizziness, Gastric Ulcer, Gastritis, Occult Blood Positive
Adverse event resulted in: hospitalization
Suspect drug(s):
Methotrexate
Dosage: 25 mg;weekly;oral
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2006-02-08
Naprosyn
Dosage: 500 mg;twice a day; oral
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2006-01-31
End date: 2006-08-25
Prednisone 50mg TAB
Dosage: 50 mg; every other day; oral
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2006-06-30
Other drugs received by patient: Folic Acid; Lansoprazole
Adverse event in 15 year old female receiving Naprosyn (Naproxen)
Reported by a individual with unspecified qualification from United States on 2007-04-03
Patient: 15 year old female
Adverse reactions / side effects: Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Methotrexate
Dosage: 25 mg/week
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2006-02-08
Naprosyn
Dosage: 500 mg bid
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2006-01-31
End date: 2006-08-25
Prednisone Tablets, 50mg
Dosage: 50 mg, qod
Administration route: Oral
Indication: Juvenile Arthritis
Start date: 2006-06-30
Unspecified Clinical Trial Drug
Indication: Juvenile Arthritis
Start date: 2006-05-04
Other drugs received by patient: Folic Acid; Prevacid
Adverse event in female receiving Naprosyn (Naproxen)
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):
Aleve
Indication: Osteoarthritis
Motrin
Indication: Osteoarthritis
Naprosyn
Administration route: Oral
Indication: Osteoarthritis
Adverse event in 73 year old female receiving Naprosyn (Naproxen)
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
Adverse event in 49 year old male receiving Naprosyn (Naproxen)
Reported by a physician from Germany on 2007-01-10
Patient: 49 year old male
Adverse reactions / side effects: Abdominal Pain, Haemoglobin Decreased, Rectal Haemorrhage
Adverse event resulted in: hospitalization
Suspect drug(s):
Naprosyn (Naproxen)
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