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From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes, said the Institute of Medicine report, released yesterday.
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Total Naproxen reports: 156.
Naproxen FDA safety alerts: 2002 2004 .
Reported deaths: 34    Reported hospitalizations: 91.
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FDA Reported Naproxen Side Effects: gastrointestinal haemorrhage, caesarean section, nausea, renal failure acute, completed suicide, dizziness, disseminated intravascular coagulation, gastritis erosive, haematocrit decreased, haemoglobin decreased, upper gastrointestinal haemorrhage.
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Showing 1-100 of 156 Next >

Naproxen Side Effects Report #5132509-X
Consumer or non-health professional from NETHERLANDS reported NAPROXEN problem on Oct 09, 2006. Female patient, 43 years of age, weighting 130.1 lb, was diagnosed with rheumatoid arthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: chest pain, dyspnoea exertional. NAPROXEN dosage: 1000 MG, ORAL. During the same period patient was treated with PLAQUENIL, KEPPRA. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5132542-8
NAPROXEN problem was reported by a Health Professional from GERMANY on Sept 13, 2006. Female patient, weighting 4.19 lb, was diagnosed with myalgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: apgar score low, caesarean section, candida sepsis, dialysis, disseminated intravascular coagulation, foetal growth retardation, foetal movements decreased. NAPROXEN dosage: unknown. Patient recovered.

Naproxen Side Effects Report #5142569-8
Pharmacist from UNITED STATES reported NAPROXEN problem on Oct 31, 2006. Male patient, 58 years of age, weighting 169.8 lb, was diagnosed with arthralgia, back pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, paraesthesia, respiratory distress, throat irritation. NAPROXEN dosage: 250MG BID ORAL. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5143120-9
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Oct 31, 2006. Male patient, weighting 308.0 lb, was diagnosed with pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: lower gastrointestinal haemorrhage. NAPROXEN dosage: 375MG TWICE A DAY PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5202768-3
Consumer or non-health professional from UNITED STATES reported NAPROXEN problem on Mar 31, 2006. Male patient, 40 years of age, was diagnosed with sinusitis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: asthenia, blood pressure increased, headache, heart rate increased, thirst, wheezing. NAPROXEN dosage: 500 MG, ORAL. During the same period patient was treated with AVELOX, SYNTHROID, AZULFIDINE, ZETIA, ZYRTEC, HUMALOG, LISINOPRIL, SINGULAIR. Patient recovered.

Naproxen Side Effects Report #5147640-2
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Nov 08, 2006. Male patient, 85 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: gastric ulcer, upper gastrointestinal haemorrhage. NAPROXEN dosage: unknown. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5151235-4
Pharmacist from UNITED STATES reported NAPROXEN problem on Nov 13, 2006. Male patient, 77 years of age, weighting 224.0 lb, was diagnosed with inflammation, pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, hyponatraemia. NAPROXEN dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5152317-3
NAPROXEN problem was reported by a Physician from GERMANY on Nov 07, 2006. Female patient, 63 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: alcohol use, intentional overdose. NAPROXEN dosage: unknown. During the same period patient was treated with ETHANOL. Patient died.

Naproxen Side Effects Report #5153262-X
Health Professional from GERMANY reported NAPROXEN problem on Nov 06, 2006. Female patient, 79 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: completed suicide, intentional overdose. NAPROXEN dosage: unknown. During the same period patient was treated with VERAPAMIL, GLUCOSAMINE. Patient died.

Naproxen Side Effects Report #5156775-X
NAPROXEN problem was reported by a Consumer or non-health professional from TURKEY on Oct 31, 2006. Female patient, 27 years of age, was diagnosed with myalgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: caesarean section, foetal growth retardation, foetal movements decreased, oligohydramnios, premature labour. NAPROXEN dosage: 1100 MG QDAY UNK. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5156776-1
Physician from TURKEY reported NAPROXEN problem on Oct 31, 2006. Female patient, weighting 4.19 lb, was diagnosed with complication of pregnancy, myalgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: anuria, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased, caesarean section, disseminated intravascular coagulation in newborn. NAPROXEN dosage: 1100 MG QDAY UNK. Patient was hospitalized. Patient died.

Naproxen Side Effects Report #5157971-8
NAPROXEN problem was reported by a Consumer or non-health professional from on Nov 21, 2006. Female patient, 27 years of age, was diagnosed with myalgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: caesarean section, oligohydramnios. NAPROXEN dosage: 1100 MG/DAY. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Naproxen Side Effects Report #5157974-3
Consumer or non-health professional from reported NAPROXEN problem on Nov 21, 2006. Female patient, weighting 4.19 lb, was diagnosed with candidiasis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: abdominal distension, anuria, caesarean section, candida sepsis, candidiasis, disseminated intravascular coagulation, fungal peritonitis. NAPROXEN dosage: MOTHER TOOK 1100 MG/DAY DURING SECOND TRIMESTER. During the same period patient was treated with FLUCONAZOLE. Patient was hospitalized. Patient died.

Naproxen Side Effects Report #5159106-4
NAPROXEN problem was reported by a Physician from UNITED STATES on Oct 24, 2006. Female patient, 79 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: completed suicide. NAPROXEN dosage: unknown. During the same period patient was treated with VERAPAMIL, GLUCOSAMINE. Patient died.

Naproxen Side Effects Report #5159107-6
Physician from UNITED STATES reported NAPROXEN problem on Oct 24, 2006. Female patient, 63 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: completed suicide. NAPROXEN dosage: unknown. During the same period patient was treated with ETHANOL. Patient died.

Naproxen Side Effects Report #5159109-X
NAPROXEN problem was reported by a Physician from UNITED STATES on Oct 24, 2006. Female patient, 55 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: completed suicide. NAPROXEN dosage: unknown. During the same period patient was treated with ASPIRIN, CARISOPRODOL. Patient died.

Naproxen Side Effects Report #5159110-6
Physician from UNITED STATES reported NAPROXEN problem on Oct 24, 2006. Female patient, 77 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: completed suicide. NAPROXEN dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient died.

Naproxen Side Effects Report #5163669-2
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Nov 27, 2006. Female patient, weighting 213.8 lb, was diagnosed with musculoskeletal pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood potassium increased. NAPROXEN dosage: 220MG TID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5164298-7
Consumer or non-health professional from UNITED STATES reported NAPROXEN problem on Nov 29, 2006. Female patient, 60 years of age, weighting 180.0 lb, was diagnosed with inflammation, pain in extremity and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: chest pain, hyperhidrosis, nausea, pulse absent. NAPROXEN dosage: unknown. Patient died on 10/20/2006.

Naproxen Side Effects Report #5165744-5
NAPROXEN problem was reported by a Health Professional from POLAND on Nov 13, 2006. Female patient, 30 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: erythema multiforme, nasal congestion, pulmonary oedema, shock. NAPROXEN dosage: unknown. During the same period patient was treated with IBUPROFEN, CELECOXIB, ASPIRIN. Patient recovered.

Naproxen Side Effects Report #5165762-7
Physician from POLAND reported NAPROXEN problem on Nov 14, 2006. Female patient, 30 years of age, was diagnosed with allergy test and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, allergy test positive, flushing, forced expiratory volume decreased, heart rate increased, hypersensitivity, nasal disorder, pulmonary oedema. NAPROXEN dosage: unknown. During the same period patient was treated with IBUPROFEN, ASPIRIN, CELECOXIB. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5166005-0
NAPROXEN problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 10, 2006. Male patient, 82 years of age, weighting 180.0 lb, was diagnosed with pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: gastric perforation, haemorrhage, kidney perforation, loss of consciousness. NAPROXEN dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5164030-7
Consumer or non-health professional from reported NAPROXEN problem on Nov 28, 2006. Female patient, 56 years of age, was diagnosed with rheumatoid arthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: gastric disorder, gastrointestinal haemorrhage, intestinal diaphragm disease, intestinal obstruction, nausea. NAPROXEN dosage: unknown. During the same period patient was treated with ROFECOXIB. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5167653-4
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Dec 01, 2006. Male patient, 62 years of age, weighting 165.0 lb, was diagnosed with back pain, sciatica, cerebrovascular accident and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: anaemia, angina pectoris, chest pain, duodenal ulcer, duodenitis, gastritis, melaena, oesophagitis, upper gastrointestinal haemorrhage. NAPROXEN dosage: 500 MG BID PO. During the same period patient was treated with ASPIRIN, ATENOLOL, CAPSAICIN CREAM, DOXEPIN, GABAPENTIN, HYDROCODONE BITARTRATE. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5168888-7
Consumer or non-health professional from UNITED STATES reported NAPROXEN problem on Dec 06, 2006. Female patient, 83 years of age, weighting 136.9 lb, was diagnosed with osteoarthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: dehydration, mycobacterium avium complex infection, renal failure acute. NAPROXEN dosage: 375 MG ORAL TID. Patient recovered.

Naproxen Side Effects Report #5171163-8
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Dec 07, 2006. Male patient, 48 years of age, weighting 164.0 lb, was diagnosed with musculoskeletal pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction. NAPROXEN dosage: 250 MG ONE BID PO. Patient recovered.

Naproxen Side Effects Report #5192688-5
Consumer or non-health professional from European Union reported NAPROXEN problem on Dec 05, 2006. Female patient was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: sepsis, upper gastrointestinal haemorrhage. NAPROXEN dosage: unknown. During the same period patient was treated with ADCAL, FRUSEMIDE, ISOSORBIDE, PERINDOPRIL ERBUMINE, RISPERIDONE, ZOPICLONE. Patient died.

Naproxen Side Effects Report #5196461-3
NAPROXEN problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 12, 2006. Male patient, 26 years of age, was diagnosed with tonsillitis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: rhabdomyolysis. NAPROXEN dosage: 1000 MG (500 MG,2 IN 1 D). During the same period patient was treated with PHENETHICILLIN POTASSIUM, AUGMENTIN. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5328434-1
Pharmacist from UNITED STATES reported NAPROXEN problem on May 16, 2007. Male patient, 66 years of age, weighting 158.7 lb, was diagnosed with arthralgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: arthralgia, blood pressure decreased, dizziness, erosive duodenitis, faeces discoloured, gastritis erosive, occult blood positive, pain in extremity. NAPROXEN dosage: 500 MG BID -PT TOOK MORE- PO. During the same period patient was treated with GABAPENTIN, ALLOPURINOL, SERTRALINE. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5386832-4
NAPROXEN problem was reported by a Consumer or non-health professional from on July 09, 2007. Female patient, 68 years of age, was diagnosed with osteoarthritis, hypertension, urinary tract infection and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: cardiac failure congestive, electrocardiogram change, fluid overload, gastrointestinal disorder, hepatic failure, nausea, overdose. NAPROXEN dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE, PREDNISONE, METHYLSULFONYLMETHANE, LEVOFLOXACIN. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5387793-4
Consumer or non-health professional from UNITED KINGDOM reported NAPROXEN problem on July 04, 2007. Male patient, 47 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: colitis ischaemic, large intestine perforation, peritonitis, sepsis. NAPROXEN dosage: 500 MG; QD; PO. During the same period patient was treated with PREGABALIN, NORTRIPTYLINE, BUPRENORPHINE, TRAMADOL. Patient recovered.

Naproxen Side Effects Report #5388067-8
NAPROXEN problem was reported by a Health Professional from UNITED KINGDOM on July 05, 2007. Male patient, 47 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: colitis ischaemic, large intestine perforation, peritonitis, sepsis. NAPROXEN dosage: unknown. During the same period patient was treated with BUPRENORPHINE, NORTRIPTYLINE, PREGABALIN, TRAMADOL. Patient was hospitalized and became disabled. Patient recovered.

Naproxen Side Effects Report #5395128-6
Pharmacist from JAPAN reported NAPROXEN problem on July 09, 2007. Male patient, 70 years of age, was diagnosed with pyrexia, insomnia, convulsion prophylaxis, constipation, neurogenic bladder, sputum retention and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: liver disorder, oculomucocutaneous syndrome, sepsis. NAPROXEN dosage: UNIT DOSE: 100 MG. During the same period patient was treated with ROHYPNOL, CERCINE, AMOBAN, MAGMITT, PHENOBARBITAL, MYSLEE, UBRETID, SPELEAR. Patient died on 10/12/2006.

Naproxen Side Effects Report #5397452-X
NAPROXEN problem was reported by a Pharmacist from JAPAN on July 09, 2007. Male patient, 70 years of age, was diagnosed with pyrexia, insomnia, convulsion prophylaxis, constipation, neurogenic bladder, sputum retention and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: liver disorder, oculomucocutaneous syndrome, sepsis. NAPROXEN dosage: UNIT DOSE: 100 MG. During the same period patient was treated with ROHYPNOL, CERCINE, AMOBAN, MAGMITT, PHENOBARBITAL, MYSLEE, UBRETID, SPELEAR. Patient died on 10/12/2006.

Naproxen Side Effects Report #5401509-4
Physician from JAPAN reported NAPROXEN problem on July 23, 2007. Male patient, 70 years of age, weighting 132.3 lb, was diagnosed with pyrexia, convulsion prophylaxis, hypertension and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: liver disorder, sepsis, stevens-johnson syndrome. NAPROXEN dosage: unknown. During the same period patient was treated with ROHYPNOL, CERCINE, PERDIPINE, AMOBAN. Patient died on 10/12/2006.

Naproxen Side Effects Report #5401526-4
NAPROXEN problem was reported by a Health Professional from SINGAPORE on July 23, 2007. Male patient, 16 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: face oedema, rhonchi. NAPROXEN dosage: unknown. Patient recovered.

Naproxen Side Effects Report #5403879-X
Pharmacist from UNITED STATES reported NAPROXEN problem on July 31, 2007. Male patient, 54 years of age, was diagnosed with pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: alcohol use, duodenal ulcer, haemorrhage. NAPROXEN dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5402820-3
NAPROXEN problem was reported by a Physician from GERMANY on July 23, 2007. Female patient, 77 years of age, was diagnosed with atrial fibrillation and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage. NAPROXEN dosage: unknown. During the same period patient was treated with WARFARIN. Patient died.

Naproxen Side Effects Report #5404199-X
Physician from JAPAN reported NAPROXEN problem on July 23, 2007. Male patient, 70 years of age, weighting 132.3 lb, was diagnosed with pyrexia, convulsion prophylaxis, hypertension and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: liver disorder, sepsis, stevens-johnson syndrome. NAPROXEN dosage: unknown. During the same period patient was treated with ROHYPNOL, CERCINE, PERDIPINE, AMOBAN. Patient died on 10/12/2006.

Naproxen Side Effects Report #5406977-X
NAPROXEN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 03, 2007. Male patient, 14 years of age, weighting 146.0 lb, was diagnosed with pain in extremity and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: cough, dyspnoea, hypersensitivity, rash, swelling. NAPROXEN dosage: unknown. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5408119-3
Consumer or non-health professional from UNITED STATES reported NAPROXEN problem on Aug 06, 2007. Male patient, 81 years of age, was diagnosed with arthralgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: gastric haemorrhage, renal impairment. NAPROXEN dosage: 375MG BID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5409293-5
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Aug 07, 2007. Male patient, 66 years of age, was diagnosed with osteoarthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: dehydration, diarrhoea, haemodialysis, nausea, renal failure acute, vomiting. NAPROXEN dosage: 220 MG DAILY PO. During the same period patient was treated with ACE INHIBITOR, PRESTARIUM, CALCIUM CITRATE, SIMETHICONE, INDAPAMIDE. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5415010-5
Pharmacist from FINLAND reported NAPROXEN problem on July 30, 2007. Female patient, 82 years of age, was diagnosed with arthralgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: epistaxis. NAPROXEN dosage: 500 MG; BID; PO. During the same period patient was treated with PROPRANOLOL, ESTRADIOL. Patient recovered.

Naproxen Side Effects Report #5419551-6
NAPROXEN problem was reported by a Health Professional from UNITED STATES on Aug 08, 2007. Female patient, 79 years of age, weighting 166.0 lb, was diagnosed with osteoarthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: renal failure. NAPROXEN dosage: unknown. During the same period patient was treated with NEXIUM, ADALAT, LIPITOR, DIPHENHYDRAMINE HYDROCHLORIDE, TYLENOL, ZESTRIL, DIHYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient died on 08/01/2007.

Naproxen Side Effects Report #5426062-0
Pharmacist from UNITED STATES reported NAPROXEN problem on Aug 24, 2007. Male patient, 63 years of age, was diagnosed with osteoarthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: anaemia, gastric haemorrhage, gastritis, gastrointestinal ulcer. NAPROXEN dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5426220-5
NAPROXEN problem was reported by a Physician from UNITED KINGDOM on Aug 17, 2007. Male patient, child 10 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: renal failure acute, renal tubular necrosis. NAPROXEN dosage: unknown. During the same period patient was treated with GENTAMICIN, DICLOFENAC, LAXATIVE NOS. Patient recovered.

Naproxen Side Effects Report #5427506-0
Pharmacist from UNITED STATES reported NAPROXEN problem on Aug 24, 2007. Male patient, 68 years of age, was diagnosed with pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: alcoholism, duodenal ulcer. NAPROXEN dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5444975-0
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Sept 04, 2007. Female patient, 28 years of age, was diagnosed with back pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: overdose, respiratory disorder, swollen tongue. NAPROXEN dosage: unknown. During the same period patient was treated with MOTRIN. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5449741-8
Pharmacist from UNITED STATES reported NAPROXEN problem on Sept 07, 2007. Female patient, 52 years of age, was diagnosed with headache and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: dizziness, gastric ulcer, haematocrit decreased, haemoglobin decreased, red blood cell count decreased, upper gastrointestinal haemorrhage. NAPROXEN dosage: 500MG TID PRN HEADACHE PO. During the same period patient was treated with IBUPROFEN, DULOXETINE, DIVALPROEX, LEVOTHYROXINE, AMLODIPINE, LABETALOL, PANTOPRAZOLE. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5455142-9
NAPROXEN problem was reported by a Pharmacist from UNITED STATES on Sept 13, 2007. Male patient, 78 years of age, was diagnosed with pain and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: renal failure acute. NAPROXEN dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5459728-7
Health Professional from UNITED KINGDOM reported NAPROXEN problem on Sept 07, 2007. Female patient, 84 years of age, weighting 202.8 lb, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood urea increased, chest pain, gastritis erosive, haematemesis, international normalised ratio increased, oesophagitis, renal failure, synovial cyst. NAPROXEN dosage: unknown. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5464342-3
NAPROXEN problem was reported by a Health Professional from UNITED KINGDOM on Sept 10, 2007. Female patient, 87 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: duodenal perforation, peritonitis. NAPROXEN dosage: unknown. During the same period patient was treated with ATORVASTATIN CALCIUM, BENDROFLUAZIDE, IRBESARTAN, PARACETAMOL, TRAMADOL. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5464348-4
Health Professional from UNITED STATES reported NAPROXEN problem on Sept 11, 2007. Female patient, 79 years of age, weighting 166.0 lb, was diagnosed with osteoarthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: clostridium difficile colitis, renal failure. NAPROXEN dosage: unknown. During the same period patient was treated with NEXIUM, ADALAT, LIPITOR, DIPHENHYDRAMINE HYDROCHLORIDE, TYLENOL, ZESTRIL, DIHYDROCHLOROTHIAZIDE, DUONEB. Patient was hospitalized. Patient died on 08/01/2007.

Naproxen Side Effects Report #5467669-4
NAPROXEN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Sept 10, 2007. Female patient, 87 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: duodenal perforation, peritonitis. NAPROXEN dosage: 500 MG; BID; PO. During the same period patient was treated with TRAMADOL, BENDROFLUMETHIAZIDE, IRBESARTAN, PARACETAMOL, ATORVASTATIN CALCIUM. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5468791-9
Consumer or non-health professional from reported NAPROXEN problem on Sept 20, 2007. Female patient, 38 years of age, was diagnosed with analgesia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: hydronephrosis, nephrectomy, nephropathy toxic, renal atrophy. NAPROXEN dosage: unknown. During the same period patient was treated with ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLOIDE, CONJUGATED ESTROGENS, METOCLOPRAMIDE, FENOFIBRATE, VENLAFAXINE, PANTOPRAZOLE. Patient recovered.

Naproxen Side Effects Report #5470159-6
NAPROXEN problem was reported by a Health Professional from UNITED STATES on Sept 11, 2007. Female patient, 38 years of age, was diagnosed with arthralgia and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: hydronephrosis, nephropathy toxic, obstructive uropathy, renal atrophy, renal impairment, renal papillary necrosis, ureteral stent insertion. NAPROXEN dosage: 325 MG DAILY,. During the same period patient was treated with PARACETAMOL, DIPHENHYDRAMINE, METOCLOPRAMIDE, FENOFIBRATE, VENLAFAXINE, PANTOPRAZOLE, HYDROCHLORIC ACID. Patient was hospitalized. Patient recovered.

Showing 1-100 of 156 Next >


Drug Information: Naproxen

URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a681029.html

(na prox' en)

IMPORTANT WARNING:

People who take nonsteroidal anti-inflammatory medications (NSAIDs) (other than aspirin) such as naproxen may have a higher risk of having a heart attack or a stroke than people who do not take these medications. These events may happen without warning and may cause death. This risk may be higher for people who take NSAIDs for a long time. Tell your doctor if you or anyone in your family has or has ever had heart disease, a heart attack, or a stroke,if you smoke, and if you have or have ever had high cholesterol, high blood pressure, or diabetes. Get emergency medical help right away if you experience any of the following symptoms: chest pain, shortness of breath, weakness in one part or side of the body, or slurred speech.If you will be undergoing a coronary artery bypass graft (CABG; a type of heart surgery), you should not take naproxen right before or right after the surgery.NSAIDs such as naproxen may cause ulcers, bleeding, or holes in the stomach or intestine. These problems may develop at any time during treatment, may happen without warning symptoms, and may cause death. The risk may be higher for people who take NSAIDs for a long time, are older in age, have poor health, or who drink three or more alcoholic drinks per day while taking naproxen. Tell your doctor if you take any of the following medications: anticoagulants ('blood thinners') such as warfarin (Coumadin); aspirin; other NSAIDs such as ibuprofen (Advil, Motrin) and ketoprofen (Orudis KT, Actron); or oral steroids such as dexamethasone (Decadron, Dexone), methylprednisolone (Medrol), and prednisone (Deltasone). Also tell your doctor if you have or have ever had ulcers, bleeding in your stomach or intestines, or other bleeding disorders. If you experience any of the following symptoms, stop taking naproxen and call your doctor: stomach pain, heartburn, vomiting a substance that is bloody or looks like coffee grounds, blood in the stool, or black and tarry stools.Keep all appointments with your doctor and the laboratory. Your doctor will monitor your symptoms carefully and will probably order certain tests to check your body's response to naproxen. Be sure to tell your doctor how you are feeling so that your doctor can prescribe the right amount of medication to treat your condition with the lowest risk of serious side effects.Your doctor or pharmacist will give you the manufacturer's patient information sheet (Medication Guide) when you begin treatment with prescription naproxen and each time you refill your prescription. Read the information carefully and ask your doctor or pharmacist if you have any questions. You can also visit the Food and Drug Administration (FDA) website (http://www.fda.gov/cder) or the manufacturer's website to obtain the Medication Guide.

Why is this medication prescribed?

Prescription naproxen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints), rheumatoid arthritis (arthritis caused by swelling of the lining of the joints), juvenile arthritis (a form of joint disease in children), and ankylosing spondylitis (arthritis that mainly affects the spine). Prescription naproxen tablets, extended-release tablets, and suspension are also used to relieve shoulder pain caused by bursitis (inflammation of a fluid-filled sac in the shoulder joint), tendinitis (inflammation of the tissue that connects muscle to bone), gouty arthritis (attacks of joint pain caused by a build-up of certain substances in the joints), and pain from other causes, including menstrual pain (pain that happens before or during a menstrual period). Nonprescription naproxen is used to reduce fever and to relieve mild pain from headaches, muscle aches, arthritis, menstrual periods, the common cold, toothaches, and backaches. Naproxen is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

How should this medicine be used?

Prescription naproxen comes as a regular tablet, an enteric coated tablet (delayed-release tablet), an extended-release (long-acting) tablet, and a suspension (liquid) to take by mouth. The extended-release tablets are usually taken once a day. The tablets, enteric coated tablets, and suspension are usually taken twice a day for arthritis. The tablets and suspension are usually taken every 8 hours for gout, and every 6-8 hours as needed for pain. If you are taking naproxen on a regular basis, you should take it at the same time(s) every day. .

Nonprescription naproxen comes as tablet and a gelatin coated tablet to take by mouth. It is usually taken with a full glass of water every 8-12 hours as needed. Nonprescription naproxen may be taken with food or milk to prevent stomach upset.

Follow the directions on the package or prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take naproxen exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor or written on the package.

Shake the liquid well before each use to mix the medication evenly. Use the measuring cup provided to measure each dose of the liquid.

Swallow the enteric coated tablets and extended release tablets whole; do not split, chew, or crush them.

If you are taking naproxen to relieve the symptoms of arthritis, your symptoms may begin to improve within 1 week. It may take 2 weeks or longer for you to feel the full benefit of the medication.

Stop taking nonprescription naproxen and call your doctor if your symptoms get worse, you develop new or unexpected symptoms, the part of your body that was painful becomes red or swollen, your pain lasts for more than 10 days, or your fever lasts for more than 3 days.

Other uses for this medicine

Naproxen is also sometimes used to treat Paget's disease of bone (a condition in which the bones become abnormally thick, fragile, and misshapen) and Bartter's syndrome (a condition in which the body does not absorb enough potassium, causing muscle cramping and weakness and other symptoms). Talk to your doctor about the risks of using this medication for your condition.

This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

What special precautions should I follow?

Before taking naproxen,

  • tell your doctor and pharmacist if you are allergic to naproxen, aspirin or other NSAIDs such as ibuprofen (Advil, Motrin) and ketoprofen (Orudis KT, Actron), any medications for pain or fever, or any other medications.
  • tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention the medications listed in the IMPORTANT WARNING section and any of the following: angiotensin-converting enzyme (ACE) inhibitors such as benazepril (Lotensin), captopril (Capoten), enalapril (Vasotec), fosinopril (Monopril), lisinopril (Prinivil, Zestril), moexipril (Univasc), perindopril (Aceon), quinapril (Accupril), ramipril (Altace), and trandolapril (Mavik); beta blockers such as atenolol (Tenormin), labetalol (Normodyne), metoprolol (Lopressor, Toprol XL), nadolol (Corgard), and propranolol (Inderal); diuretics ('water pills'); lithium (Eskalith, Lithobid), medications for diabetes, methotrexate (Rheumatrex); phenytoin (Dilantin); probenecid (Benemid); and sulfa antibiotics such as sulfisoxazole (Gantrisin) and sulfamethoxazole (in Bactrim, in Septra). If you are taking the enteric coated tablets, also tell your doctor if you are taking antacids or sucralfate (Carafate). Your doctor may need to change the doses of your medication or monitor you more carefully for side effects.
  • do not take nonprescription naproxen with any other medication for pain unless your doctor tells you that you should.
  • tell your doctor if you have been told to follow a low sodium diet and if you have or have ever had any of the conditions mentioned in the IMPORTANT WARNING section or asthma, especially if you also have frequent stuffed or runny nose or nasal polyps (swelling of the inside of the nose); swelling of the hands, arms, feet, ankles, or lower legs;anemia (red blood cells do not bring enough oxygen to all parts of the body); or liver or kidney disease.
  • tell your doctor if you are pregnant, especially if you are in the last few months of your pregnancy, you plan to become pregnant, or you are breast-feeding. If you become pregnant while taking naproxen, call your doctor.
  • if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking naproxen.
  • you should know that this medication may make you dizzy, drowsy, or depressed. Do not drive a car or operate machinery until you know how this drug affects you.
  • remember that alcohol can add to the drowsiness caused by this medication. .

What special dietary instructions should I follow?

Unless your doctor tells you otherwise, continue your normal diet.

What should I do if I forget a dose?

Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.

What side effects can this medication cause?

Naproxen may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

  • constipation
  • diarrhea
  • gas
  • sores in mouth
  • excessive thirst
  • headache
  • dizziness
  • lightheadedness
  • drowsiness
  • difficulty falling asleep or staying asleep
  • burning or tingling in the arms or legs
  • cold symptoms
  • ringing in the ears
  • hearing problems

Some side effects can be serious. If you experience any of the following symptoms, or those mentioned in the IMPORTANT WARNING section, call your doctor immediately. Do not take any more naproxen until you speak to your doctor:

  • changes in vision
  • feeling that the tablet is stuck in your throat
  • unexplained weight gain
  • sore throat, fever, chills, and other signs of infection
  • blisters
  • rash
  • skin reddening
  • itching
  • hives
  • swelling of the eyes, face, lips, tongue, throat, arms, hands, feet, ankles, or lower legs
  • difficulty breathing or swallowing
  • hoarseness
  • excessive tiredness
  • pain in the upper right part of the stomach
  • upset stomach
  • loss of appetite
  • yellowing of the skin or eyes
  • flu-like symptoms
  • bruises or purple blotches under the skin
  • pale skin
  • fast heartbeat
  • cloudy, discolored, or bloody urine
  • back pain
  • difficult or painful urination

Naproxen may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].

What storage conditions are needed for this medicine?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.

In case of emergency/overdose

In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.

Symptoms of overdose may include:

  • dizziness
  • extreme tiredness
  • confusion
  • drowsiness
  • stomach pain
  • heartburn
  • upset stomach
  • vomiting
  • slow or difficult breathing
  • decreased urination

What other information should I know?

Before having any laboratory test, tell your doctor and the laboratory personnel that you are taking naproxen.

If you are taking prescription naproxen, do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.

It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.

Brand name(s):

  • Aleve®
  • Anaprox®
  • Anaprox® DS
  • EC-Naprosyn®
  • Naprelan®
  • Naprosyn®

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chest pain, dyspnoea exertional apgar score low, caesarean section, candida sepsis, dialysis, disseminated intravascular coagulation, foetal growth retardation, foetal movements decreased, was diagnosed with rheumatoid arthritis and was diagnosed with myalgia and was diagnosed with arthralgia, back pain and