RELAFEN Side Effects

6934326-4 | Chronic Obstructive Pulmonary Disease, Coronary Arterial Stent Insertion, Dehydration, Dry Eye, Dry Mouth, Dysphagia, Interstitial Lung Disease
on Aug 11, 2010 Female patient from UNITED STATES , 77 years of age, was diagnosed with pain (What is pain?), hypertension and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: chronic obstructive pulmonary disease, coronary arterial stent insertion, dehydration, dry eye, dry mouth, dysphagia, interstitial lung disease. Relafen dosage: . During the same period patient was treated with LISINOPRIL (2.5mg Per Day) (View Lisinopril Review and Lisinopril Label ), PLAQUENIL (200mg Twice Per Day) (View Plaquenil Review and Plaquenil Label ), IMURAN (View Imuran Review and Imuran Label ).

6888034-9 | Dizziness, Haematemesis
Patient was taking Relafen (View Usage). Patient had the following side effects: dizziness (What is dizziness?), haematemesis on Jul 22, 2010 from CHINA Additional patient health information: Female patient , 73 years of age, . Relafen dosage: 1tab Per Day.

6878703-9 | Dizziness, Haematemesis, Product Quality Issue
Adverse event was reported on Jul 22, 2010 by a Female patient taking Relafen (View Usage) (Dosage: 1tab Per Day) . Location: CHINA , 73 years of age, After Relafen was administered, patient had the following side effects: dizziness (What is dizziness?), haematemesis, product quality issue.

6857032-3 | Dehydration, Dry Eye, Dry Mouth, Dysphagia, Photosensitivity Reaction, Visual Acuity Reduced, Weight Decreased
on Jul 12, 2010 Female patient from UNITED STATES , 77 years of age, was diagnosed with pain (What is pain?), hypertension and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, dry eye, dry mouth, dysphagia, photosensitivity reaction, visual acuity reduced, weight decreased. Relafen dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), IMURAN (View Imuran Review and Imuran Label ).


6184948-6 | Urticaria
on Apr 11, 2008 Female patient from UNITED STATES , 67 years of age, was diagnosed with blood pressure (What is blood pressure?), arthritis (What is arthritis?) and was treated with Relafen (View Usage). Patient had the following side effects: urticaria. Relafen dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), ATENOLOL (50mg Per Day) (View Atenolol Review and Atenolol Label ), DIOVAN (320mg Per Day) (View Diovan Review and Diovan Label ), NORVASC (25mg Per Day) (View Norvasc Review and Norvasc Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), IODINE (View Iodine Review and Iodine Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ).

6122100-0 | Stevens-johnson Syndrome
Patient was taking Relafen (View Usage). After Relafen was administered, patient had the following side effects: stevens-johnson syndrome on Mar 16, 2009 from UNITED STATES Additional patient health information: Male patient , 51 years of age, weighting 180.0 lb, was diagnosed with osteoarthritis (What is osteoarthritis?) and. Relafen dosage: Po. Patient was hospitalized.

5939951-5 | Blood Pressure Increased, Burn Of Internal Organs, Convulsion, Gastric Haemorrhage, Gastrointestinal Ulcer, Injury, Myocardial Infarction, Rash
Adverse event was reported on Oct 31, 2008 by a Female patient taking Relafen (View Usage) (Dosage: 1 Per Day) was diagnosed with joint sprain, osteopenia and. Location: UNITED STATES , 65 years of age, weighting 138.0 lb, Patient experienced the following unwanted or unexpected effects: blood pressure increased, burn of internal organs, convulsion, gastric haemorrhage, gastrointestinal ulcer, injury, myocardial infarction, rash (What is rash?). During the same period patient was treated with FOSAMAX (1 Per Week) (View Fosamax Review and Fosamax Label ). Patient was hospitalized.

5887903-6 | Burning Sensation, Disability, Hypersensitivity, Joint Swelling, Oedema Peripheral, Paraesthesia, Pyrexia, Rheumatoid Arthritis
on Sep 15, 2008 Female patient from UNITED STATES , 47 years of age, was treated with Relafen (View Usage). Patient had the following side effects: burning sensation, disability, hypersensitivity, joint swelling, oedema peripheral, paraesthesia, pyrexia, rheumatoid arthritis (What is rheumatoid arthritis?). Relafen dosage: 1tab Single Dose. During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

5843105-0 | Arthralgia, Cellulitis, Dysstasia, Gait Disturbance, Joint Swelling, Musculoskeletal Pain, Oedema Peripheral, Pain In Extremity
on Aug 12, 2008 Female patient from UNITED STATES , 63 years of age, weighting 190.0 lb, was diagnosed with myalgia, neck pain and was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: arthralgia, cellulitis (What is cellulitis?), dysstasia, gait disturbance, joint swelling, musculoskeletal pain, oedema peripheral, pain in extremity. Relafen dosage: 1 500 Mg 2x Day Po.

5827140-4 | Abdominal Pain, Faeces Discoloured, Haematemesis, Liver Function Test Abnormal, Melaena
Patient was taking Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), faeces discoloured, haematemesis, liver function test abnormal, melaena on Jul 29, 2008 from UNITED STATES Additional patient health information: Female patient , 72 years of age, weighting 125.4 lb, was diagnosed with arthritis (What is arthritis?) and. Relafen dosage: 1 Bid Po.

5734424-7 | Vision Blurred, Visual Disturbance
Adverse event was reported on Mar 11, 2008 by a Female patient taking Relafen (View Usage) (Dosage: ) was diagnosed with thyroid disorder, migraine (What is migraine?) and. Location: UNITED STATES , 70 years of age, Patient had the following side effects: vision blurred, visual disturbance. During the same period patient was treated with LEVOTHROID (View Levothroid Review and Levothroid Label ), EXCEDRIN (MIGRAINE) (2tab Single Dose) (View Excedrin (migraine) Review and Excedrin (migraine) Label ).

5734421-1 | Diarrhoea, Fatigue, Flatulence
on Sep 19, 2007 Female patient from UNITED STATES , 37 years of age, was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: diarrhoea, fatigue, flatulence. Relafen dosage: 750mg Twice Per Day. During the same period patient was treated with PRAMLINTIDE (View Pramlintide Review and Pramlintide Label ), LANTUS (View Lantus Review and Lantus Label ), NOVOLOG (View Novolog Review and Novolog Label ), PIOGLITAZONE (View Pioglitazone Review and Pioglitazone Label ), OXCARBAZEPINE (View Oxcarbazepine Review and Oxcarbazepine Label ), SEROQUEL (View Seroquel Review and Seroquel Label ).

5704478-2 | Oral Mucosal Eruption, Pruritus, Rash Erythematous, Rash Pustular
on Apr 11, 2008 Female patient from UNITED STATES , weighting 200.0 lb, was diagnosed with back pain (What is back pain?), middle ear effusion and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: oral mucosal eruption, pruritus, rash erythematous, rash pustular. Relafen dosage: 2 500mg Tablets 1x Day 2/dinner Po. During the same period patient was treated with CHLORPHENIRAMINE MALEATE (Methscopolamine Nitrate 2.5mg White Am / Blue Pm Po) (View Chlorpheniramine Maleate Review and Chlorpheniramine Maleate Label ).

5690103-6 | Deafness, Spinal Cord Herniation, Tinnitus
Patient was taking Relafen (View Usage). Patient had the following side effects: deafness, spinal cord herniation, tinnitus (What is tinnitus?) on Mar 31, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 130.0 lb, was diagnosed with arthralgia and. Relafen dosage: 2 Tablets Once A Day Po.

5441416-4 | Stevens-johnson Syndrome
Adverse event was reported on Aug 28, 2007 by a Female patient taking Relafen (View Usage) (Dosage: 500mg 3x A Day Po) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: UNITED STATES , weighting 125.0 lb, After Relafen was administered, patient had the following side effects: stevens-johnson syndrome.

5364007-2 | Bradyarrhythmia, Pain
on Jun 11, 2007 Male patient from UNITED STATES , 33 years of age, was diagnosed with depression (What is depression?), pain (What is pain?) and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: bradyarrhythmia, pain (What is pain?). Relafen dosage: . During the same period patient was treated with VALIUM (View Valium Review and Valium Label ), SONATA (View Sonata Review and Sonata Label ), CYMBALTA (60 Mg, 2/d) (View Cymbalta Review and Cymbalta Label ), OXYCONTIN (80 Mg, Unk) (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (30 Mg, Unk) (View Oxycodone Hcl Review and Oxycodone Hcl Label ).

5324146-9 | Diarrhoea
on Feb 20, 2007 Male patient from UNITED STATES , 79 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Relafen (View Usage). Patient had the following side effects: diarrhoea. Relafen dosage: 500mg Per Day. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), CARDURA (View Cardura Review and Cardura Label ), PROSCAR (View Proscar Review and Proscar Label ), CARTIA XT (View Cartia Xt Review and Cartia Xt Label ), QUININE SULFATE (View Quinine Sulfate Review and Quinine Sulfate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

5324136-6 | Dyspepsia, Hyperchlorhydria, Mouth Ulceration, Oral Fungal Infection, Oral Mucosal Eruption, Stomatitis, Throat Irritation
Patient was taking Relafen (View Usage). After Relafen was administered, patient had the following side effects: dyspepsia, hyperchlorhydria, mouth ulceration, oral fungal infection, oral mucosal eruption, stomatitis, throat irritation on Oct 17, 2006 from UNITED STATES Additional patient health information: Female patient , 28 years of age, . Relafen dosage: 500mg Twice Per Day. During the same period patient was treated with ACTIQ (400mcg As Required) (View Actiq Review and Actiq Label ).

5324132-9 | Myalgia, Tinnitus
Adverse event was reported on Sep 13, 2006 by a Male patient taking Relafen (View Usage) (Dosage: 500mg Twice Per Day) was diagnosed with gout (What is gout?) and. Location: UNITED STATES , 43 years of age, Patient experienced the following unwanted or unexpected effects: myalgia, tinnitus (What is tinnitus?). During the same period patient was treated with GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ), CONDROSULF (View Condrosulf Review and Condrosulf Label ).

5324131-7 | Coeliac Disease
on Sep 11, 2006 Male patient from UNITED STATES , 46 years of age, was diagnosed with back pain (What is back pain?) and was treated with Relafen (View Usage). Patient had the following side effects: coeliac disease. Relafen dosage: .

5324128-7 | Myalgia
on Aug 15, 2006 Female patient from UNITED STATES , 66 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: myalgia. Relafen dosage: .

5324124-X | Back Disorder, Balance Disorder, Dizziness, Dyskinesia, Dyspepsia, Fall, Gait Disturbance, Ill-defined Disorder
Patient was taking Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: back disorder, balance disorder, dizziness (What is dizziness?), dyskinesia, dyspepsia, fall (What is fall?), gait disturbance, ill-defined disorder on Jul 31, 2006 from UNITED STATES Additional patient health information: Female patient , 37 years of age, was diagnosed with inflammatory pain and. Relafen dosage: . During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ).

5324112-3 | Spider Vein
Adverse event was reported on Jun 06, 2006 by a Female patient taking Relafen (View Usage) (Dosage: 500mg Variable Dose) was diagnosed with back pain (What is back pain?) and. Location: UNITED STATES , 51 years of age, Patient had the following side effects: spider vein. During the same period patient was treated with LEXAPRO (View Lexapro Review and Lexapro Label ), DARVOCET (View Darvocet Review and Darvocet Label ), LORTAB (View Lortab Review and Lortab Label ), ZOCOR (View Zocor Review and Zocor Label ).

5324100-7 | Haemorrhage
on Apr 24, 2006 Male patient from UNITED STATES , 43 years of age, was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: haemorrhage. Relafen dosage: 500mg Twice Per Day. During the same period patient was treated with NABUMETONE (View Nabumetone Review and Nabumetone Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), AVANDIA (View Avandia Review and Avandia Label ), PROTONIX (View Protonix Review and Protonix Label ), BUPROPION HYDROCHLORIDE (View Bupropion Hydrochloride Review and Bupropion Hydrochloride Label ), BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), STARLIX (View Starlix Review and Starlix Label ), VYTORIN (View Vytorin Review and Vytorin Label ).

5324097-X | Diarrhoea, Flatulence
on Apr 17, 2006 Male patient from UNITED STATES , 52 years of age, was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, flatulence. Relafen dosage: 500mg Per Day. During the same period patient was treated with NADOLOL (View Nadolol Review and Nadolol Label ), CARDURA (View Cardura Review and Cardura Label ).

5324090-7 | Dizziness, Fatigue, Feeling Abnormal
Patient was taking Relafen (View Usage). Patient had the following side effects: dizziness (What is dizziness?), fatigue, feeling abnormal on Mar 28, 2006 from UNITED STATES Additional patient health information: Female patient , 50 years of age, . Relafen dosage: 500mg Twice Per Day. During the same period patient was treated with NABUMETONE (View Nabumetone Review and Nabumetone Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

5103426-6 | Hypotension, Stevens-johnson Syndrome
Adverse event was reported on Aug 29, 2006 by a Male patient taking Relafen (View Usage) (Dosage: ) was diagnosed with myalgia and. Location: UNITED STATES , 15 years of age, After Relafen was administered, patient had the following side effects: hypotension, stevens-johnson syndrome. Patient was hospitalized.

5061449-X | Dyspnoea, Oedema Peripheral
on Jul 20, 2006 Female patient from UNITED STATES , 86 years of age, weighting 165.0 lb, was diagnosed with arthritis (What is arthritis?) and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, oedema peripheral. Relafen dosage: 500 Mg Two Daily Many Years. Patient was hospitalized.

5008638-8 | Aneurysm, Back Pain, Balance Disorder, Cerebrovascular Accident, Gait Disturbance, Nervous System Disorder
on Feb 08, 2006 Male patient from UNITED STATES , 77 years of age, was treated with Relafen (View Usage). Patient had the following side effects: aneurysm (What is aneurysm?), back pain (What is back pain?), balance disorder, cerebrovascular accident, gait disturbance, nervous system disorder. Relafen dosage: . During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ). Patient was hospitalized.

5002539-7 | Aortic Valve Incompetence, Arteriosclerosis, Blood Cholesterol Increased, Chest Pain, Contusion, Coronary Artery Disease, Dilatation Atrial, Fall, Joint Swelling
Patient was taking Relafen (View Usage). After Relafen was administered, patient had the following side effects: aortic valve incompetence, arteriosclerosis, blood cholesterol increased, chest pain (What is chest pain?), contusion, coronary artery disease (What is coronary artery disease?), dilatation atrial, fall (What is fall?), joint swelling on Jan 26, 2006 from UNITED STATES Additional patient health information: Male patient , 76 years of age, weighting 180.8 lb, was diagnosed with pain (What is pain?), arthritis (What is arthritis?), joint injury, fluid retention, hypertension, gastric disorder, erectile dysfunction (What is erectile dysfunction?), parkinson's disease (What is parkinson's disease?), dyspepsia and. Relafen dosage: . During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ), LASIX (View Lasix Review and Lasix Label ), PREVACID (View Prevacid Review and Prevacid Label ), VIAGRA (View Viagra Review and Viagra Label ), CARBIDOPA AND LEVODOPA (View Carbidopa And Levodopa Review and Carbidopa And Levodopa Label ), NEXIUM (View Nexium Review and Nexium Label ). Patient was hospitalized.

5001829-1 | Abdominal Pain Upper, Cardiac Failure Congestive, Oedema Peripheral, Pulmonary Oedema
Adverse event was reported on May 11, 2006 by a Male patient taking Relafen (View Usage) (Dosage: ) . Location: CANADA , 79 years of age, Patient experienced the following unwanted or unexpected effects: abdominal pain upper, cardiac failure congestive, oedema peripheral, pulmonary oedema. During the same period patient was treated with CELEBREX (View Celebrex Review and Celebrex Label ).

5000903-3 | Gastric Haemorrhage
on Jan 31, 2006 Female patient from UNITED STATES , 57 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Relafen (View Usage). Patient had the following side effects: gastric haemorrhage. Relafen dosage: 500mg Three Times Per Day. During the same period patient was treated with CARAFATE (View Carafate Review and Carafate Label ), NEXIUM (View Nexium Review and Nexium Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), ACTONEL (View Actonel Review and Actonel Label ), HUMIRA (View Humira Review and Humira Label ). Patient was hospitalized.

5000902-1 | Stomach Discomfort
on Jan 30, 2006 Female patient from UNITED STATES , 50 years of age, was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: stomach discomfort. Relafen dosage: .

5000901-X | Arthritis
Patient was taking Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: arthritis (What is arthritis?) on Jan 27, 2006 from UNITED STATES Additional patient health information: Female patient , 43 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Relafen dosage: .

5000897-0 | Diarrhoea
Adverse event was reported on Dec 14, 2005 by a Female patient taking Relafen (View Usage) (Dosage: 750mg Twice Per Day) was diagnosed with morton's neuroma and. Location: UNITED STATES , 61 years of age, Patient had the following side effects: diarrhoea. During the same period patient was treated with RANITIDINE (View Ranitidine Review and Ranitidine Label ), IMODIUM (View Imodium Review and Imodium Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), PAMELOR (View Pamelor Review and Pamelor Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), ULTRAM (View Ultram Review and Ultram Label ), ZOCOR (View Zocor Review and Zocor Label ), TRENTAL (View Trental Review and Trental Label ).

5000894-5 | Mobility Decreased
on Oct 25, 2005 Female patient from UNITED STATES , 71 years of age, weighting 138.2 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: mobility decreased. Relafen dosage: 500mg Three Times Per Day. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), INDAPAMIDE (View Indapamide Review and Indapamide Label ), PREMARIN (View Premarin Review and Premarin Label ), CLARITIN (View Claritin Review and Claritin Label ), K DUR 10 (View K-dur 10 Review and K-dur 10 Label ).

5000892-1 | Dysphagia, Dysphonia, Musculoskeletal Stiffness, Paraesthesia
on Oct 14, 2005 Female patient from UNITED STATES , 77 years of age, weighting 100.3 lb, was diagnosed with osteoarthritis (What is osteoarthritis?), incontinence and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: dysphagia, dysphonia, musculoskeletal stiffness, paraesthesia. Relafen dosage: 500mg Twice Per Day. During the same period patient was treated with ASPIRIN (81mg Per Day) (View Aspirin Review and Aspirin Label ), FLONASE (1spr Per Day) (View Flonase Review and Flonase Label ), IMIPRAMINE (10mg Per Day) (View Imipramine Review and Imipramine Label ).

5000890-8 | Somnolence
Patient was taking Relafen (View Usage). Patient had the following side effects: somnolence on Sep 22, 2005 from UNITED STATES Additional patient health information: Female patient , 46 years of age, . Relafen dosage: 500mg Three Times Per Day. During the same period patient was treated with PERCOCET (View Percocet Review and Percocet Label ), LEXAPRO (View Lexapro Review and Lexapro Label ).

5000887-8 | Migraine With Aura
Adverse event was reported on Aug 19, 2005 by a Female patient taking Relafen (View Usage) (Dosage: 1000mg Per Day) was diagnosed with osteoarthritis (What is osteoarthritis?) and. Location: UNITED STATES , 67 years of age, After Relafen was administered, patient had the following side effects: migraine with aura.

5000885-4 | Rash
on Jul 06, 2005 Female patient from UNITED STATES , 50 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: rash (What is rash?). Relafen dosage: .

5000883-0 | Skin Irritation, Vaginal Swelling
on Jun 27, 2005 Female patient from UNITED STATES , 47 years of age, weighting 126.3 lb, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Relafen (View Usage). Patient had the following side effects: skin irritation, vaginal swelling. Relafen dosage: 500mg Per Day. During the same period patient was treated with PLAQUENIL (200mg Twice Per Day) (View Plaquenil Review and Plaquenil Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), RENPRESS (1tab Per Day) (View Renpress Review and Renpress Label ), SULFASALAZINE (500mg Six Times Per Day) (View Sulfasalazine Review and Sulfasalazine Label ).

5000878-7 | Arthralgia, Joint Stiffness, Myalgia
Patient was taking Relafen (View Usage). After Relafen was administered, patient had the following side effects: arthralgia, joint stiffness, myalgia on Apr 29, 2005 from UNITED STATES Additional patient health information: Female patient , 53 years of age, . Relafen dosage: 500mg Twice Per Day. During the same period patient was treated with ZYPREXA (View Zyprexa Review and Zyprexa Label ), WELLBUTRIN SR (View Wellbutrin Sr Review and Wellbutrin Sr Label ), TRIAMTERENE (View Triamterene Review and Triamterene Label ), NORTRIPTYLINE HCL (View Nortriptyline Hcl Review and Nortriptyline Hcl Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), ZETIA (View Zetia Review and Zetia Label ).

5000877-5 | Bladder Pain, Nausea
Adverse event was reported on Apr 29, 2005 by a Female patient taking Relafen (View Usage) (Dosage: 750mg Twice Per Day) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: UNITED STATES , 72 years of age, Patient experienced the following unwanted or unexpected effects: bladder pain, nausea (What is nausea?). During the same period patient was treated with EXTRA STRENGTH TYLENOL (View Extra Strength Tylenol Review and Extra Strength Tylenol Label ), MACROBID (View Macrobid Review and Macrobid Label ), TARKA (View Tarka Review and Tarka Label ), VICODIN (View Vicodin Review and Vicodin Label ).

5000876-3 | Dyspepsia, Fluid Retention, Weight Increased
on Apr 27, 2005 Female patient from UNITED STATES , 50 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Relafen (View Usage). Patient had the following side effects: dyspepsia, fluid retention, weight increased. Relafen dosage: 750mg Per Day. During the same period patient was treated with AZULFIDINE (View Azulfidine Review and Azulfidine Label ), PREVACID (View Prevacid Review and Prevacid Label ).

5000875-1 | Asthma
on Apr 18, 2005 Female patient from UNITED STATES , 42 years of age, was diagnosed with fibromyalgia and was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: asthma (What is asthma?). Relafen dosage: 750mg Twice Per Day. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ).

5000873-8 | Urticaria
Patient was taking Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: urticaria on Apr 06, 2005 from UNITED STATES Additional patient health information: Female patient , 68 years of age, was diagnosed with back pain (What is back pain?) and. Relafen dosage: 1000mg Per Day. During the same period patient was treated with ATACAND (View Atacand Review and Atacand Label ), IMIPRAMINE (View Imipramine Review and Imipramine Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), OSCAL (View Oscal Review and Oscal Label ).

5000872-6 | Tinnitus
Adverse event was reported on Mar 29, 2005 by a Female patient taking Relafen (View Usage) (Dosage: 1g Per Day) was diagnosed with osteoarthritis (What is osteoarthritis?) and. Location: UNITED STATES , 54 years of age, Patient had the following side effects: tinnitus (What is tinnitus?). During the same period patient was treated with ESTROGENS SOL/INJ (View Estrogens Sol/inj Review and Estrogens Sol/inj Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5000870-2 | Somnolence
on Mar 23, 2005 Female patient from UNITED STATES , 50 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Relafen (View Usage). After Relafen was administered, patient had the following side effects: somnolence. Relafen dosage: 750mg Twice Per Day. During the same period patient was treated with M.V.I. (View M.v.i. Review and M.v.i. Label ), CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ).

4986342-X | Retinal Tear, Vision Blurred, Visual Disturbance
on Mar 29, 2006 Female patient from CANADA , 60 years of age, weighting 144.4 lb, was treated with Relafen (View Usage). Patient experienced the following unwanted or unexpected effects: retinal tear, vision blurred, visual disturbance. Relafen dosage: 500mg Twice Per Day. During the same period patient was treated with PREVACID (30mg Per Day) (View Prevacid Review and Prevacid Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

4979981-3 | Aortic Valve Incompetence, Arteriosclerosis, Asthenia, Cardiac Failure Congestive, Cardio-respiratory Arrest, Cerebrovascular Accident, Chronic Obstructive Pulmonary Disease, Dilatation Atrial, Dilatation Ventricular
Patient was taking Relafen (View Usage). Patient had the following side effects: aortic valve incompetence, arteriosclerosis, asthenia, cardiac failure congestive, cardio-respiratory arrest, cerebrovascular accident, chronic obstructive pulmonary disease, dilatation atrial, dilatation ventricular on Jul 21, 2005 from UNITED STATES Additional patient health information: Female patient , 52 years of age, weighting 121.3 lb, was diagnosed with arthritis (What is arthritis?) and. Relafen dosage: . During the same period patient was treated with TRIMETHOPRIM (View Trimethoprim Review and Trimethoprim Label ), ZITHROMAX (View Zithromax Review and Zithromax Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), VIOXX (View Vioxx Review and Vioxx Label ), ACYCLOVIR (View Acyclovir Review and Acyclovir Label ), AGGRENOX (View Aggrenox Review and Aggrenox Label ), VENTOLIN (View Ventolin Review and Ventolin Label ), ARAVA (View Arava Review and Arava Label ). Patient was hospitalized and became disabled.