KETOPROFEN Side Effects

6815398-4 | Constipation, Diarrhoea, Feeling Abnormal, Hypoaesthesia, Neuropathy Peripheral, Therapeutic Response Unexpected, Vomiting
on Jun 21, 2010 Male patient from UNITED KINGDOM , 64 years of age, weighting 235.9 lb, was diagnosed with arthritis (What is arthritis?), bronchopulmonary aspergillosis and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: constipation (What is constipation?), diarrhoea, feeling abnormal, hypoaesthesia, neuropathy peripheral, therapeutic response unexpected, vomiting. Ketoprofen dosage: . During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), CELECOXIB (View Celecoxib Review and Celecoxib Label ), VORICONAZOLE (View Voriconazole Review and Voriconazole Label ).

6786392-7 | Constipation, Diarrhoea, Feeling Abnormal, Hypoaesthesia, Neuropathy Peripheral, Therapeutic Response Unexpected, Vomiting
Patient was taking Ketoprofen (View Usage). Patient had the following side effects: constipation (What is constipation?), diarrhoea, feeling abnormal, hypoaesthesia, neuropathy peripheral, therapeutic response unexpected, vomiting on Jun 18, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 64 years of age, weighting 235.9 lb, was diagnosed with arthritis (What is arthritis?), bronchopulmonary aspergillosis and. Ketoprofen dosage: . During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), CELECOXIB (View Celecoxib Review and Celecoxib Label ), VORICONAZOLE (View Voriconazole Review and Voriconazole Label ).

6779029-4 | Constipation, Diarrhoea, Feeling Abnormal, Neuropathy Peripheral
Adverse event was reported on Jun 03, 2010 by a Male patient taking Ketoprofen (View Usage) (Dosage: ) was diagnosed with arthritis (What is arthritis?), bronchopulmonary aspergillosis and. Location: UNITED KINGDOM , 64 years of age, weighting 235.9 lb, After Ketoprofen was administered, patient had the following side effects: constipation (What is constipation?), diarrhoea, feeling abnormal, neuropathy peripheral. During the same period patient was treated with CELEBREX (View Celebrex Review and Celebrex Label ), TRAMADOL (View Tramadol Review and Tramadol Label ), VORICONAZOLE (View Voriconazole Review and Voriconazole Label ).

6763999-4 | Constipation, Diarrhoea, Feeling Abnormal, Hypoaesthesia, Neuropathy Peripheral, Therapeutic Response Unexpected, Vomiting
on Jun 04, 2010 Male patient from UNITED KINGDOM , 64 years of age, weighting 235.9 lb, was diagnosed with arthritis (What is arthritis?), bronchopulmonary aspergillosis and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: constipation (What is constipation?), diarrhoea, feeling abnormal, hypoaesthesia, neuropathy peripheral, therapeutic response unexpected, vomiting. Ketoprofen dosage: . During the same period patient was treated with TRAMADOL (View Tramadol Review and Tramadol Label ), CELECOXIB (View Celecoxib Review and Celecoxib Label ), VORICONAZOLE (View Voriconazole Review and Voriconazole Label ).


6655301-3 | Confusional State, Constipation, Dysuria, Malaise, Nightmare, Orthostatic Hypotension
on Mar 15, 2010 Female patient from FRANCE , 82 years of age, was treated with Ketoprofen (View Usage). Patient had the following side effects: confusional state, constipation (What is constipation?), dysuria, malaise, nightmare, orthostatic hypotension. Ketoprofen dosage: . During the same period patient was treated with STILNOX (View Stilnox Review and Stilnox Label ), ACTISKENAN (View Actiskenan Review and Actiskenan Label ), DURAGESIC 100 (View Duragesic-100 Review and Duragesic-100 Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), LAMALINE (Dose:1 Unit(s)) (View Lamaline Review and Lamaline Label ), DEROXAT (View Deroxat Review and Deroxat Label ), SINEMET (View Sinemet Review and Sinemet Label ), REQUIP (View Requip Review and Requip Label ). Patient was hospitalized.

6634736-9 | Renal Failure Acute
Patient was taking Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: renal failure acute on Mar 09, 2010 from FRANCE Additional patient health information: Male patient , 67 years of age, . Ketoprofen dosage: . During the same period patient was treated with LASILIX (View Lasilix Review and Lasilix Label ), NEXIUM /UNK/ (View Nexium /unk/ Review and Nexium /unk/ Label ), APROVEL (View Aprovel Review and Aprovel Label ), HYZAAR (View Hyzaar Review and Hyzaar Label ), AMLOR (View Amlor Review and Amlor Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

6577083-6 | Renal Failure Acute
Adverse event was reported on Feb 02, 2010 by a Male patient taking Ketoprofen (View Usage) (Dosage: ) . Location: FRANCE , 67 years of age, Patient experienced the following unwanted or unexpected effects: renal failure acute. During the same period patient was treated with LASILIX (View Lasilix Review and Lasilix Label ), NEXIUM /UNK/ (View Nexium /unk/ Review and Nexium /unk/ Label ), APROVEL (View Aprovel Review and Aprovel Label ), HYZAAR (View Hyzaar Review and Hyzaar Label ), AMLOR (View Amlor Review and Amlor Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

6550456-3 | Gastrointestinal Haemorrhage, Myocardial Infarction
on Jan 15, 2010 Female patient from SWEDEN , 92 years of age, was treated with Ketoprofen (View Usage). Patient had the following side effects: gastrointestinal haemorrhage, myocardial infarction. Ketoprofen dosage: .

6414381-0 | Eye Swelling, Lip Swelling, Oedema Peripheral, Swelling Face
on Oct 13, 2009 Male patient from CROATIA (local name: Hrvatska) , 63 years of age, was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: eye swelling, lip swelling, oedema peripheral, swelling face. Ketoprofen dosage: 150 Mg/day, Oral. During the same period patient was treated with MEDROL (View Medrol Review and Medrol Label ), IRUZID (HYDROCHLOROTHIAZIDE, LISINOPRIL) (View Iruzid (hydrochlorothiazide, Lisinopril) Review and Iruzid (hydrochlorothiazide, Lisinopril) Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6366285-X | Atrioventricular Block Complete, Syncope
Patient was taking Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: atrioventricular block complete, syncope on Sep 08, 2009 from FRANCE Additional patient health information: Female patient , 43 years of age, was diagnosed with sciatica (What is sciatica?), systemic lupus erythematosus and. Ketoprofen dosage: Unk. During the same period patient was treated with DEXTROPROPOXYPHAN (Unk) (View Dextropropoxyphan Review and Dextropropoxyphan Label ), CHLOROQUINE PHOSPHATE (4 Mg/kg/day) (View Chloroquine Phosphate Review and Chloroquine Phosphate Label ). Patient was hospitalized.

6346708-2 | Asthenia, Decompression Sickness, Decreased Activity
Adverse event was reported on Aug 27, 2009 by a Male patient taking Ketoprofen (View Usage) (Dosage: ; Oral) was diagnosed with headache (What is headache?) and. Location: SLOVENIA , 44 years of age, Patient had the following side effects: asthenia, decompression sickness, decreased activity.

6295681-4 | Decreased Appetite, Dyspepsia, Epigastric Discomfort, Faeces Pale, Hepatitis Cholestatic, Sinusitis
on Aug 03, 2009 Male patient from UNITED STATES , 65 years of age, was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: decreased appetite, dyspepsia, epigastric discomfort, faeces pale, hepatitis cholestatic, sinusitis (What is sinusitis?). Ketoprofen dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ), SULFAMETHOXAZOLE AND TRIMETHOPRIM (View Sulfamethoxazole And Trimethoprim Review and Sulfamethoxazole And Trimethoprim Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

6295681-4 | Decreased Appetite, Dyspepsia, Epigastric Discomfort, Faeces Pale, Hepatitis Cholestatic, Sinusitis
on Aug 03, 2009 Male patient from UNITED STATES , 65 years of age, was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: decreased appetite, dyspepsia, epigastric discomfort, faeces pale, hepatitis cholestatic, sinusitis (What is sinusitis?). Ketoprofen dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ), SULFAMETHOXAZOLE AND TRIMETHOPRIM (View Sulfamethoxazole And Trimethoprim Review and Sulfamethoxazole And Trimethoprim Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

6262507-4 | Application Site Burn, Burns Second Degree, Dermatitis Bullous
Patient was taking Ketoprofen (View Usage). Patient had the following side effects: application site burn, burns second degree, dermatitis bullous on Jun 26, 2009 from FRANCE Additional patient health information: Male patient , 37 years of age, weighting 154.3 lb, was diagnosed with arthralgia and. Ketoprofen dosage: . During the same period patient was treated with AERIUS (View Aerius Review and Aerius Label ).

6253401-3 | Petechiae
Adverse event was reported on May 27, 2009 by a Male patient taking Ketoprofen (View Usage) (Dosage: ) . Location: SWEDEN , 81 years of age, After Ketoprofen was administered, patient had the following side effects: petechiae. During the same period patient was treated with DEXIBUPROFEN (View Dexibuprofen Review and Dexibuprofen Label ).

6168326-1 | Hyperkalaemia
on Apr 15, 2009 Female patient from POLAND , 80 years of age, weighting 141.1 lb, was diagnosed with osteoarthritis (What is osteoarthritis?), hypertension and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: hyperkalaemia. Ketoprofen dosage: 200 Mg Oral. During the same period patient was treated with POTASSIUM CHLORIDE (2250 Mgoral) (View Potassium Chloride Review and Potassium Chloride Label ), INHIBACE (0.5 Mg Oral) (View Inhibace Review and Inhibace Label ), ASPARGIN (ASPARTIC ACID) (1500 Mg Oral) (View Aspargin (aspartic Acid) Review and Aspargin (aspartic Acid) Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6028040-X | Duodenal Ulcer
on Dec 22, 2008 Female patient from UNITED KINGDOM , 54 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Ketoprofen (View Usage). Patient had the following side effects: duodenal ulcer. Ketoprofen dosage: 100 Mg, Oral. During the same period patient was treated with NSULIN (INSULIN) (View Nsulin (insulin) Review and Nsulin (insulin) Label ).

5978032-1 | Renal Failure Acute
Patient was taking Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: renal failure acute on Nov 14, 2008 from POLAND Additional patient health information: Female patient , 84 years of age, weighting 127.9 lb, was diagnosed with osteoarthritis (What is osteoarthritis?), hypertension and. Ketoprofen dosage: 100 Mg, Tid, Oral. During the same period patient was treated with MEFENAMIC ACID (250 Mg, Tid, Oral) (View Mefenamic Acid Review and Mefenamic Acid Label ), PERINDOPRIL ERBUMINE (4 Mg/day, Oral) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), DIGOXIN (View Digoxin Review and Digoxin Label ).

5875754-8 | Stevens-johnson Syndrome
Adverse event was reported on Aug 29, 2008 by a Female patient taking Ketoprofen (View Usage) (Dosage: ) . Location: ITALY , 83 years of age, Patient experienced the following unwanted or unexpected effects: stevens-johnson syndrome. Patient was hospitalized.

5809949-6 | Convulsion, Disturbance In Attention, Fall, Fatigue, Renal Impairment
on Jul 11, 2008 Male patient from CANADA , 47 years of age, was diagnosed with neuralgia, diabetes mellitus and was treated with Ketoprofen (View Usage). Patient had the following side effects: convulsion, disturbance in attention, fall (What is fall?), fatigue, renal impairment. Ketoprofen dosage: . During the same period patient was treated with PREGABALIN (View Pregabalin Review and Pregabalin Label ), METFORMIN (View Metformin Review and Metformin Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ). Patient was hospitalized.

5804357-6 | Convulsion, Disturbance In Attention, Fall, Fatigue, Renal Impairment
on Apr 10, 2008 Male patient from CANADA , 47 years of age, was diagnosed with neuralgia, diabetes mellitus and was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: convulsion, disturbance in attention, fall (What is fall?), fatigue, renal impairment. Ketoprofen dosage: . During the same period patient was treated with PREGABALIN (View Pregabalin Review and Pregabalin Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ). Patient was hospitalized.

5800884-6 | Anaemia, Gastric Haemorrhage, Haematemesis, Thrombocytopenia
Patient was taking Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, gastric haemorrhage, haematemesis, thrombocytopenia on Jun 17, 2008 from UNITED STATES Additional patient health information: Male patient , 58 years of age, weighting 178.6 lb, was diagnosed with pain (What is pain?) and. Ketoprofen dosage: 150 Mg; Twice A Day; Oral. During the same period patient was treated with SUNITINIB MALATE (SUNITINIB MALATE) (50 MG) (50 Mg; Daily; Oral, 50 Mg; Daily; Oral) (View Sunitinib Malate (sunitinib Malate) (50 Mg) Review and Sunitinib Malate (sunitinib Malate) (50 Mg) Label ), COLCHICINE (View Colchicine Review and Colchicine Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), SANDOSTATINE /00821001/ (View Sandostatine /00821001/ Review and Sandostatine /00821001/ Label ), ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE TABLETS, USP (View Enalapril Maleate And Hydrochlorothiazide Tablets, Usp Review and Enalapril Maleate And Hydrochlorothiazide Tablets, Usp Label ), LACTULOSE (View Lactulose Review and Lactulose Label ). Patient was hospitalized.

5761024-5 | Cerebral Haemorrhage, Necrotising Enterocolitis Neonatal, Neonatal Respiratory Distress Syndrome
Adverse event was reported on May 28, 2008 by a Male patient taking Ketoprofen (View Usage) (Dosage: ) . Location: , weighting 2.71 lb, Patient had the following side effects: cerebral haemorrhage, necrotising enterocolitis neonatal, neonatal respiratory distress syndrome. During the same period patient was treated with FLAGYL (View Flagyl Review and Flagyl Label ), MIFEGYNE (View Mifegyne Review and Mifegyne Label ), CYTOTEC (View Cytotec Review and Cytotec Label ), LOXEN (View Loxen Review and Loxen Label ), CELESTENE /00008501/ (View Celestene /00008501/ Review and Celestene /00008501/ Label ), CLAMOXYL /00249601/ (View Clamoxyl /00249601/ Review and Clamoxyl /00249601/ Label ). Patient was hospitalized.

5709176-7 | Convulsion, Disturbance In Attention, Fall, Fatigue, Renal Impairment
on Apr 07, 2008 Male patient from CANADA , 47 years of age, was diagnosed with neuralgia, diabetes mellitus and was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: convulsion, disturbance in attention, fall (What is fall?), fatigue, renal impairment. Ketoprofen dosage: . During the same period patient was treated with PREGABALIN (View Pregabalin Review and Pregabalin Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ). Patient was hospitalized.

5605654-X | Angioedema, Dyspnoea, Pyrexia
on Jan 09, 2008 Female patient from SWEDEN , 36 years of age, was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, dyspnoea, pyrexia. Ketoprofen dosage: ; Oral. Patient was hospitalized.

5580659-6 | Optic Neuritis Retrobulbar
Patient was taking Ketoprofen (View Usage). Patient had the following side effects: optic neuritis retrobulbar on Dec 26, 2007 from FRANCE Additional patient health information: Male patient , 58 years of age, was diagnosed with arthralgia and. Ketoprofen dosage: Unk. During the same period patient was treated with PLAQUENIL (Unk) (View Plaquenil Review and Plaquenil Label ). Patient was hospitalized.

5515775-8 | Blood Creatinine Increased, Blood Urea Increased, Glucose Urine Present, Nausea, Urinary Casts, Urine Ketone Body Present
Adverse event was reported on Oct 26, 2007 by a Male patient taking Ketoprofen (View Usage) (Dosage: Oral) was diagnosed with arthralgia, gout (What is gout?) and. Location: POLAND , 50 years of age, weighting 220.5 lb, After Ketoprofen was administered, patient had the following side effects: blood creatinine increased, blood urea increased, glucose urine present, nausea (What is nausea?), urinary casts, urine ketone body present. During the same period patient was treated with DICLOFENAC SODIUM (Oral) (View Diclofenac Sodium Review and Diclofenac Sodium Label ), AULIN ^MEDICOM^(NIMESULIDE) (View Aulin ^medicom^(nimesulide) Review and Aulin ^medicom^(nimesulide) Label ). Patient was hospitalized.

5463003-4 | Schamberg's Disease
on Sep 18, 2007 Female patient from UNITED STATES , 75 years of age, weighting 150.0 lb, was diagnosed with arthritis (What is arthritis?) and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: schamberg's disease. Ketoprofen dosage: Cutaneous.

5400476-7 | Staphylococcal Infection, Toxic Epidermal Necrolysis
on Jul 13, 2007 Female patient from ITALY , 94 years of age, was diagnosed with influenza like illness and was treated with Ketoprofen (View Usage). Patient had the following side effects: staphylococcal infection (What is staphylococcal infection?), toxic epidermal necrolysis. Ketoprofen dosage: . Patient was hospitalized.

5400463-9 | Toxic Epidermal Necrolysis, Wound Infection Staphylococcal
Patient was taking Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: toxic epidermal necrolysis, wound infection staphylococcal on Jul 13, 2007 from ITALY Additional patient health information: Male patient , 31 years of age, was diagnosed with systemic lupus erythematosus and. Ketoprofen dosage: . During the same period patient was treated with CARBAMAZEPINE (View Carbamazepine Review and Carbamazepine Label ). Patient was hospitalized.

5390868-7 | Blister, Dermatitis Contact, Wound Secretion
Adverse event was reported on Jul 03, 2007 by a Female patient taking Ketoprofen (View Usage) (Dosage: Tid, Topical) was diagnosed with pain (What is pain?) and. Location: POLAND , 53 years of age, weighting 198.4 lb, Patient experienced the following unwanted or unexpected effects: blister, dermatitis contact, wound secretion. During the same period patient was treated with OLFEN (DICLOFENAC SODIUM) (View Olfen (diclofenac Sodium) Review and Olfen (diclofenac Sodium) Label ). Patient was hospitalized.

5301554-3 | Anaesthetic Complication, Diarrhoea, Po2 Decreased, Procedural Hypotension, Procedural Vomiting
on Apr 02, 2007 Male patient from UNITED KINGDOM , 54 years of age, weighting 249.1 lb, was diagnosed with perioperative analgesia and was treated with Ketoprofen (View Usage). Patient had the following side effects: anaesthetic complication, diarrhoea, po2 decreased, procedural hypotension, procedural vomiting. Ketoprofen dosage: 100 Mg, Once/single, Oral. During the same period patient was treated with RANITIDINE (150 Mg, Oral) (View Ranitidine Review and Ranitidine Label ), DEXAMETHASONE TAB (4 Mg, Once/single, Intravenous) (View Dexamethasone Tab Review and Dexamethasone Tab Label ), MIDAZOLAM HCL (1 Mg, Once/single, Intravenous) (View Midazolam Hcl Review and Midazolam Hcl Label ), OXYGEN(OXYGEN) (View Oxygen(oxygen) Review and Oxygen(oxygen) Label ), PROPOFOL (1 Df, Once/single, Intravenous) (View Propofol Review and Propofol Label ), REMIFENTANIL(REMIFENTANIL) (1df, Once/single, Intravenous) (View Remifentanil(remifentanil) Review and Remifentanil(remifentanil) Label ), TRAMADOL HCL (100 Mg, Once/single, Intravenous) (View Tramadol Hcl Review and Tramadol Hcl Label ), CHLORPHENIRAMINE TAB (View Chlorpheniramine Tab Review and Chlorpheniramine Tab Label ).

5153201-1 | Swollen Tongue
on Oct 31, 2006 Male patient from DENMARK , 78 years of age, weighting 132.3 lb, was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: swollen tongue. Ketoprofen dosage: Oral.

5129317-2 | Haemorrhagic Diathesis, Thrombocytopenia
Patient was taking Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhagic diathesis, thrombocytopenia on Oct 11, 2006 from POLAND Additional patient health information: Female patient , 58 years of age, . Ketoprofen dosage: .

5128822-2 | Haemorrhagic Diathesis, Thrombocytopenia
Adverse event was reported on Oct 11, 2006 by a Female patient taking Ketoprofen (View Usage) (Dosage: ) . Location: POLAND , 58 years of age, Patient had the following side effects: haemorrhagic diathesis, thrombocytopenia.

5126520-2 | Abdominal Pain, Blood Pressure Decreased, Dizziness, Haemorrhagic Stroke, Hypertension, Neuropathy
on Sep 26, 2006 Female patient from UNITED STATES , 71 years of age, weighting 120.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), blood pressure decreased, dizziness (What is dizziness?), haemorrhagic stroke, hypertension, neuropathy. Ketoprofen dosage: 200 Mg Variable Po. During the same period patient was treated with PREMARIN (View Premarin Review and Premarin Label ), VASOTEC (View Vasotec Review and Vasotec Label ). Patient was hospitalized and became disabled.

5093618-7 | Abdominal Pain Upper, Fall, Haemorrhagic Stroke, Hypotension
on Aug 16, 2006 Female patient from UNITED STATES , 71 years of age, weighting 120.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, fall (What is fall?), haemorrhagic stroke, hypotension. Ketoprofen dosage: 200 Mg Variable Po. During the same period patient was treated with PREMARIN (View Premarin Review and Premarin Label ), VASOTEC (View Vasotec Review and Vasotec Label ). Patient was hospitalized and became disabled.

4967514-7 | Abdominal Pain, Duodenitis, Haematemesis, Rectal Haemorrhage, Ulcer, Weight Decreased
Patient was taking Ketoprofen (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), duodenitis, haematemesis, rectal haemorrhage, ulcer (What is ulcer?), weight decreased on Apr 07, 2006 from UNITED STATES Additional patient health information: Female patient , 13 years of age, weighting 94.00 lb, was diagnosed with headache (What is headache?) and. Ketoprofen dosage: One Capsule Once At Night. Patient was hospitalized.

4947860-3 | Abdominal Pain Upper, Cardiac Failure Congestive, Condition Aggravated, Dyspnoea, Exercise Tolerance Decreased, Gravitational Oedema
Adverse event was reported on Feb 27, 2006 by a Female patient taking Ketoprofen (View Usage) (Dosage: 300 Mg, Qd, Oral) was diagnosed with intercostal neuralgia and. Location: POLAND , 80 years of age, weighting 132.3 lb, After Ketoprofen was administered, patient had the following side effects: abdominal pain upper, cardiac failure congestive, condition aggravated, dyspnoea, exercise tolerance decreased, gravitational oedema. During the same period patient was treated with DICLOREUM(DICLOFENAC SODIUM) (200 Mg, Qd, Oral) (View Dicloreum(diclofenac Sodium) Review and Dicloreum(diclofenac Sodium) Label ), CAPTOPRIL (View Captopril Review and Captopril Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), SPIRONOL (SPIRONOLACTONE) (View Spironol (spironolactone) Review and Spironol (spironolactone) Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ). Patient was hospitalized.

4885923-1 | Leukocytoclastic Vasculitis, Vascular Purpura
on Jan 04, 2006 Male patient from FRANCE , 73 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: leukocytoclastic vasculitis, vascular purpura. Ketoprofen dosage: . During the same period patient was treated with ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ). Patient was hospitalized.

4875669-8 | Leukocytoclastic Vasculitis
on Dec 24, 2005 Male patient from FRANCE , 73 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Ketoprofen (View Usage). Patient had the following side effects: leukocytoclastic vasculitis. Ketoprofen dosage: . During the same period patient was treated with ROFECOXIB (50 Mg, Qd) (View Rofecoxib Review and Rofecoxib Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ). Patient was hospitalized.

4810944-4 | Hyperkalaemia, Renal Impairment
Patient was taking Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: hyperkalaemia, renal impairment on Oct 20, 2005 from FRANCE Additional patient health information: Female patient , 59 years of age, was diagnosed with pain in extremity, sciatica (What is sciatica?), cardiomyopathy (What is cardiomyopathy?) and. Ketoprofen dosage: Controlled/modified. During the same period patient was treated with RAMIPRIL (View Ramipril Review and Ramipril Label ), ALDACTAZINE (View Aldactazine Review and Aldactazine Label ), ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ). Patient was hospitalized.

4774506-X | Dermatitis Allergic, Purpura, Rash
Adverse event was reported on Sep 08, 2005 by a Male patient taking Ketoprofen (View Usage) (Dosage: See Image) was diagnosed with tenosynovitis and. Location: CZECH REPUBLIC , 58 years of age, Patient experienced the following unwanted or unexpected effects: dermatitis allergic, purpura, rash (What is rash?). During the same period patient was treated with FLAVOBION (SILYBUM MARIANUM) (View Flavobion (silybum Marianum) Review and Flavobion (silybum Marianum) Label ).

4725830-8 | Haematemesis
on Jul 22, 2005 Male patient from UNITED STATES , 54 years of age, weighting 136.2 lb, was diagnosed with cancer pain, gastrooesophageal reflux disease, peptic ulcer (What is peptic ulcer?) and was treated with Ketoprofen (View Usage). Patient had the following side effects: haematemesis. Ketoprofen dosage: 75 Mg Bid. During the same period patient was treated with ZANTAC (150 Mg) (View Zantac Review and Zantac Label ). Patient was hospitalized.

4694103-4 | Conjunctivitis, Dyspnoea, Toxic Epidermal Necrolysis, Urticaria
on Jun 08, 2005 Male patient from , 21 years of age, weighting 176.4 lb, was diagnosed with pain in extremity and was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: conjunctivitis, dyspnoea, toxic epidermal necrolysis, urticaria. Ketoprofen dosage: 50 Mg, Oral. During the same period patient was treated with NUTRITION SUPPLEMENTS (NUTRITION SUPPLEMENTS0 (View Nutrition Supplements (nutrition Supplements0 Review and Nutrition Supplements (nutrition Supplements0 Label ), ALCOHOL (ETHANOL) (View Alcohol (ethanol) Review and Alcohol (ethanol) Label ). Patient was hospitalized.

4647485-3 | Gastric Ulcer Haemorrhage
Patient was taking Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: gastric ulcer haemorrhage on Apr 26, 2005 from Additional patient health information: Male patient , 87 years of age, weighting 176.4 lb, was diagnosed with back pain (What is back pain?) and. Ketoprofen dosage: 300 Mg. During the same period patient was treated with RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ). Patient was hospitalized.

4639649-X | Gastrointestinal Haemorrhage
Adverse event was reported on Mar 30, 2005 by a Female patient taking Ketoprofen (View Usage) (Dosage: 200 Mg, Oral) was diagnosed with back pain (What is back pain?) and. Location: , weighting 198.4 lb, Patient had the following side effects: gastrointestinal haemorrhage. During the same period patient was treated with INDOMETHACIN (150 Mg, Oral) (View Indomethacin Review and Indomethacin Label ), VINOPTIN (VINPOCETINE) (View Vinoptin (vinpocetine) Review and Vinoptin (vinpocetine) Label ), SELGIN (SELEGILINE HYDROCHLORIDE) (View Selgin (selegiline Hydrochloride) Review and Selgin (selegiline Hydrochloride) Label ), MELOKSAM (MELOXICAM) (30 Mg,) (View Meloksam (meloxicam) Review and Meloksam (meloxicam) Label ). Patient was hospitalized.

4597027-6 | Barrett's Oesophagus, Gastric Ulcer, Gastritis Erosive, Haematemesis
on Feb 14, 2005 Male patient from , 67 years of age, was diagnosed with spinal osteoarthritis and was treated with Ketoprofen (View Usage). After Ketoprofen was administered, patient had the following side effects: barrett's oesophagus, gastric ulcer, gastritis erosive, haematemesis. Ketoprofen dosage: 200 Mg, Qd, Oral. During the same period patient was treated with ROFECOXIB (12.5 Mg, Oral) (View Rofecoxib Review and Rofecoxib Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), BENDROFLUAZIDE (BENDROFLUAZIDE) (View Bendrofluazide (bendrofluazide) Review and Bendrofluazide (bendrofluazide) Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ). Patient was hospitalized.

4596489-8 | B-cell Lymphoma
on Feb 18, 2005 Female patient from , 57 years of age, was diagnosed with systemic lupus erythematosus and was treated with Ketoprofen (View Usage). Patient experienced the following unwanted or unexpected effects: b-cell lymphoma. Ketoprofen dosage: Unk. During the same period patient was treated with CORTANCYL (Unk) (View Cortancyl Review and Cortancyl Label ), PLAQUENIL (600 Mg) (View Plaquenil Review and Plaquenil Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ). Patient was hospitalized.

4593970-2 | Barrett's Oesophagus, Gastric Ulcer, Gastritis Erosive, Haematemesis
Patient was taking Ketoprofen (View Usage). Patient had the following side effects: barrett's oesophagus, gastric ulcer, gastritis erosive, haematemesis on Feb 14, 2005 from Additional patient health information: Male patient , 67 years of age, was diagnosed with spinal osteoarthritis and. Ketoprofen dosage: 200 Mg, Qd, Oral. During the same period patient was treated with ROFECOXIB (12.5 Mg, Oral) (View Rofecoxib Review and Rofecoxib Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), BENDROFLUAZIDE (BENDROFLUMETHIAZIDE) (View Bendrofluazide (bendroflumethiazide) Review and Bendrofluazide (bendroflumethiazide) Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ). Patient was hospitalized.