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Index of reports
> Cases resulting in a serious event (38)
> Cases with Dyspnoea (7)
Below is the selection of adverse event reports related to Naprosyn (Naproxen) that includes cases resulting in a serious event where reactions include dyspnoea.
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 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 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 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 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 35 year old female receiving Naprosyn (Naproxen)
Reported by a pharmacist from Canada on 2007-02-20
Patient: 35 year old female, weighing 94.0 kg (206.8 pounds)
Adverse reactions / side effects: Burning Sensation, Speech Disorder, Dyspnoea, Tongue Oedema, Blindness Transient
Suspect drug(s):
Flagyl
Start date: 2002-05-20
End date: 2002-05-22
Naprosyn
Administration route: Oral
Start date: 2002-05-20
End date: 2002-05-22
Tylenol W / Codeine NO. 3
Dosage: dose: 1.5 dosage form
Start date: 2002-05-21
End date: 2002-05-22
Other drugs received by patient: Gentamicin Sulfate; Methyldopa; Docusate Sodium; Acetaminophen
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