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Naprosyn (Naproxen) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Naprosyn (Naproxen). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (38)
     Dyspnoea (7)Gastrointestinal Haemorrhage (5)Pain (4)more >>

Cases resulting in a serious event (38)
     Dyspnoea (7)Gastrointestinal Haemorrhage (5)Pain (4)more >>

Cases resulting in death (4)
     Contusion (2)Dyspnoea (2)Abnormal Behaviour (2)more >>

Cases resulting in life threatening events (1)
     Hiatus Hernia (1)Pain (1)Stomach Discomfort (1)more >>

Cases resulting in hospitalization (20)
     Dyspnoea (6)Gastrointestinal Haemorrhage (5)Drug Interaction (4)more >>

Cases resulting in disability (1)
     Cataract (1)Sweat Gland Disorder (1)Coma (1)more >>

Cases resulting in other serious reactions (17)
     Pain (4)Nausea (3)Skin Exfoliation (3)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Naprosyn (Naproxen). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in female receiving Naprosyn (Naproxen)

Reported by a individual with unspecified qualification from United States on 2007-10-25

Patient: female, weighing 81.0 kg (178.2 pounds)

Adverse reactions / side effects: Hypersensitivity, Urticaria

Suspect drug(s):
Chantix
    Administration route: Oral
    Indication: Smoking Cessation Therapy
    Start date: 2007-08-11
    End date: 2007-08-27

Naprosyn

Prednisone



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 54 year old female receiving Naprosyn (Naproxen)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: 54 year old female

Adverse reactions / side effects: Spinal Fracture, RIB Fracture

Suspect drug(s):
Boniva
    Indication: Osteoporosis
    Start date: 2007-06-01

Naprosyn

Other drugs received by patient: Celexa; Coumadin; Flexeril; Florinef; Glyburide; Lasix; Librax; Lidoderm; Lorcet; Maxzide; Methadone HCL; Metolazone; Neurontin; Nifedipine; Potassium CL; Prednisone; Xanax; Zetia; Cleocin Hydrochloride



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 19 year old female receiving Naprosyn (Naproxen)

Reported by a consumer/non-health professional from Germany on 2007-07-05

Patient: 19 year old female

Adverse reactions / side effects: Drug Ineffective, Vaginal Haemorrhage

Suspect drug(s):
Naprosyn (Naproxen)

Other drugs received by patient: Clomipramine HCL; Clonazepam



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 53 year old male receiving Naprosyn (Naproxen)

Reported by a consumer/non-health professional from United States on 2007-04-13

Patient: 53 year old male

Adverse reactions / side effects: Myocardial Infarction

Adverse event resulted in: death

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 34 year old female receiving Naprosyn (Naproxen)

Reported by a pharmacist from Canada on 2007-03-29

Patient: 34 year old female, weighing 83.0 kg (182.6 pounds)

Adverse reactions / side effects: Skin Exfoliation, Vulval Disorder, Pain, Dermatitis Bullous, Rash Scarlatiniform

Suspect drug(s):
Amoxil
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Naprosyn
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Alesse; Reactine; Atarax; Opticrom; Ventolin; Advil; Zantac; Flovent; Imovane; Citalopram Hydrobromide



Adverse event in 34 year old female receiving Naprosyn (Naproxen)

Reported by a pharmacist from Canada on 2007-03-28

Patient: 34 year old female

Adverse reactions / side effects: Skin Exfoliation, Vulval Disorder, Pain, Dermatitis Bullous, Rash Scarlatiniform

Suspect drug(s):
Amoxil
    Administration route: Oral

Naprosyn
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Alesse; Reactine; Opticrom; Ventolin; Zantac; Imovane; Citalopram Hydrobromide; Flovent; Advil



Adverse event in 48 year old male receiving Naprosyn (Naproxen)

Reported by a consumer/non-health professional from Canada on 2007-03-27

Patient: 48 year old male

Adverse reactions / side effects: Death, Blood Urea Increased, Renal Tubular Necrosis, Blood Creatinine Increased, Hypercalcaemia, Renal Failure Acute

Adverse event resulted in: death

Suspect drug(s):
Naprosyn
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Viread
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Quinine; Pantoprazole Sodium; Spironolactone; Septra DS; Kaletra; Videx; Furosemide; Kayexalate; 1 Concomitant Drug



Adverse event in 43 year old female receiving Naprosyn (Naproxen)

Reported by a health professional (non-physician/pharmacist) from Canada on 2007-03-26

Patient: 43 year old female

Adverse reactions / side effects: Electrocardiogram QT Prolonged, Blood Alcohol Increased, Metabolic Acidosis, Restlessness, Intentional Overdose, Hypotension, Loss of Consciousness, Leukocytosis

Suspect drug(s):
Naprosyn (Naproxen)

Other drugs received by patient: Alcohol; Plaquenil

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