ARAVA Side Effects

7020345-9 | Anaemia, Bone Marrow Toxicity, Leukopenia
on Sep 20, 2010 Female patient from SPAIN , 42 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, bone marrow toxicity, leukopenia. Arava dosage: .

7020262-4 | Ascites, Cardiac Failure, Hepatic Cirrhosis, Pericardial Effusion
Patient was taking Arava (View Usage). Patient had the following side effects: ascites, cardiac failure, hepatic cirrhosis, pericardial effusion on Sep 20, 2010 from GERMANY Additional patient health information: Male patient , 63 years of age, weighting 158.7 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with HYALURONATE SODIUM (View Hyaluronate Sodium Review and Hyaluronate Sodium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ). Patient was hospitalized.

7020086-8 | Acute Myocardial Infarction
Adverse event was reported on Jul 14, 2010 by a Male patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: JAPAN , 71 years of age, After Arava was administered, patient had the following side effects: acute myocardial infarction. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), KLARICID (View Klaricid Review and Klaricid Label ), AZULFIDINE (View Azulfidine Review and Azulfidine Label ), VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

7017756-4 | Abasia, Alopecia, Amnesia, Arthralgia, Asthenia, Dizziness, Myalgia
on Sep 21, 2010 Female patient from UNITED STATES , 56 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: abasia, alopecia, amnesia, arthralgia, asthenia, dizziness (What is dizziness?), myalgia. Arava dosage: .


7012406-5 | Constipation, Decreased Appetite, Dysphagia, Headache, Hepatotoxicity, Hyperhidrosis, Jaundice, Nausea, Pruritus
on Sep 10, 2010 Female patient from UNITED STATES , 54 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient had the following side effects: constipation (What is constipation?), decreased appetite, dysphagia, headache (What is headache?), hepatotoxicity, hyperhidrosis, jaundice (What is jaundice?), nausea (What is nausea?), pruritus. Arava dosage: . During the same period patient was treated with HERBAL PREPARATION (View Herbal Preparation Review and Herbal Preparation Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ACTONEL (View Actonel Review and Actonel Label ), ALTACE (View Altace Review and Altace Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ).

7012399-0 | Activated Partial Thromboplastin Time Prolonged, Coagulopathy, Ecchymosis, Hepatic Enzyme Increased, Prothrombin Time Prolonged
Patient was taking Arava (View Usage). After Arava was administered, patient had the following side effects: activated partial thromboplastin time prolonged, coagulopathy, ecchymosis, hepatic enzyme increased, prothrombin time prolonged on Sep 10, 2010 from UNITED STATES Additional patient health information: Female patient , 56 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ). Patient was hospitalized.

7012346-1 | Abdominal Tenderness, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Cholelithiasis, Chromaturia, Faeces Pale, Fatigue, Jaundice Cholestatic, Vomiting Projectile
Adverse event was reported on Sep 10, 2010 by a Female patient taking Arava (View Usage) (Dosage: 100 Mg/day For Three Days Followed By Maintenance Dose Of 10 Mg Daily For Rheumatoid Arthritis) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), psoriasis, postmenopause and. Location: UNITED STATES , 86 years of age, weighting 143.3 lb, Patient experienced the following unwanted or unexpected effects: abdominal tenderness, blood alkaline phosphatase increased, blood bilirubin increased, cholelithiasis, chromaturia, faeces pale, fatigue, jaundice cholestatic, vomiting projectile. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), CLINORIL (View Clinoril Review and Clinoril Label ), PREMARIN (1.25 Mg On Monday, Wednesday, And Friday) (View Premarin Review and Premarin Label ), HUMULIN N (Dose:20 Unit(s)) (View Humulin N Review and Humulin N Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ). Patient was hospitalized.

7012302-3 | Acute Hepatic Failure
on Sep 10, 2010 Female patient from UNITED STATES , 58 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient had the following side effects: acute hepatic failure. Arava dosage: . During the same period patient was treated with LOVASTATIN (View Lovastatin Review and Lovastatin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), TRAMADOL (View Tramadol Review and Tramadol Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ).

7012283-2 | Dyspnoea, Jaundice, Liver Injury, Nausea, Oedema
on Sep 21, 2010 Female patient from FRANCE , 60 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: dyspnoea, jaundice (What is jaundice?), liver injury, nausea (What is nausea?), oedema. Arava dosage: . Patient was hospitalized.

7009299-9 | Blood Alkaline Phosphatase Increased, Jaundice, Transaminases Increased
Patient was taking Arava (View Usage). Patient experienced the following unwanted or unexpected effects: blood alkaline phosphatase increased, jaundice (What is jaundice?), transaminases increased on Sep 10, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 182.5 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . Patient was hospitalized.

7009286-0 | Liver Function Test Abnormal, Pneumonia, Sepsis
Adverse event was reported on Sep 10, 2010 by a Male patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: UNITED STATES , 55 years of age, weighting 174.2 lb, Patient had the following side effects: liver function test abnormal, pneumonia (What is pneumonia?), sepsis (What is sepsis?). During the same period patient was treated with VERELAN (View Verelan Review and Verelan Label ), CLARITIN (View Claritin Review and Claritin Label ), LEVOFLOXACIN (View Levofloxacin Review and Levofloxacin Label ). Patient was hospitalized.

7009285-9 | Hepatotoxicity
on Sep 10, 2010 Female patient from UNITED STATES , 64 years of age, was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: hepatotoxicity. Arava dosage: . During the same period patient was treated with ACTIGALL (View Actigall Review and Actigall Label ), AMBIEN (View Ambien Review and Ambien Label ), VISTARIL (View Vistaril Review and Vistaril Label ), ACTONEL (View Actonel Review and Actonel Label ), VITAMIN TAB (View Vitamin Tab Review and Vitamin Tab Label ).

7009264-1 | Hepatotoxicity, Hypophagia, Malaise, Myalgia, Nausea
on Sep 10, 2010 Female patient from UNITED STATES , weighting 14.33 lb, was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: hepatotoxicity, hypophagia, malaise, myalgia, nausea (What is nausea?). Arava dosage: Duration- Approximately 3-4 Weeks.. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), FERROUS SULFATE (View Ferrous Sulfate Review and Ferrous Sulfate Label ), VIOXX (View Vioxx Review and Vioxx Label ), PREVACID (View Prevacid Review and Prevacid Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ). Patient was hospitalized.

7009255-0 | Acute Hepatic Failure, Acute Myocardial Infarction, Hepatitis B, Jaundice, Liver Function Test Abnormal, Renal Failure Acute
Patient was taking Arava (View Usage). Patient had the following side effects: acute hepatic failure, acute myocardial infarction, hepatitis b (What is hepatitis b?), jaundice (What is jaundice?), liver function test abnormal, renal failure acute on Sep 10, 2010 from UNITED STATES Additional patient health information: Male patient , 69 years of age, weighting 185.2 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with METHOTREXATE (Lifetime Dose } 1800 Mg) (View Methotrexate Review and Methotrexate Label ), DIFLUNISAL (View Diflunisal Review and Diflunisal Label ). Patient was hospitalized.

7009253-7 | Hepatitis Fulminant
Adverse event was reported on Sep 10, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) . Location: AUSTRALIA , 48 years of age, After Arava was administered, patient had the following side effects: hepatitis fulminant. During the same period patient was treated with EFFEXOR (View Effexor Review and Effexor Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), ARTANE (View Artane Review and Artane Label ), KLACID (View Klacid Review and Klacid Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), MOBIC (View Mobic Review and Mobic Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), ZYPREXA (View Zyprexa Review and Zyprexa Label ). Patient was hospitalized.

7009252-5 | Cardiac Arrest, Coma Hepatic, Hepatic Failure, Jaundice
on Sep 10, 2010 Female patient from UNITED STATES , 54 years of age, was diagnosed with psoriasis and was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?), coma hepatic, hepatic failure, jaundice (What is jaundice?). Arava dosage: . During the same period patient was treated with REMICADE (Total 3 Infusions, 300 Mg Each, Iv Drip Every 8 Weeks) (View Remicade Review and Remicade Label ).

7009249-5 | Ascites, Asthenia, Fatigue, Hepatitis, Hepatotoxicity, Jaundice, Liver Function Test Abnormal, Malaise
on Sep 10, 2010 Male patient from UNITED STATES , 54 years of age, was treated with Arava (View Usage). Patient had the following side effects: ascites, asthenia, fatigue, hepatitis (What is hepatitis?), hepatotoxicity, jaundice (What is jaundice?), liver function test abnormal, malaise. Arava dosage: . During the same period patient was treated with PLAQUENIL (View Plaquenil Review and Plaquenil Label ), IPRATROPIUM BROMIDE/SALBUTAMOL SULFATE (View Ipratropium Bromide/salbutamol Sulfate Review and Ipratropium Bromide/salbutamol Sulfate Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), METRONIDAZOLE (View Metronidazole Review and Metronidazole Label ), PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

7009248-3 | Diarrhoea, Hepatic Enzyme Increased, Nausea, Weight Decreased
Patient was taking Arava (View Usage). After Arava was administered, patient had the following side effects: diarrhoea, hepatic enzyme increased, nausea (What is nausea?), weight decreased on Sep 10, 2010 from UNITED STATES Additional patient health information: Male patient , 64 years of age, weighting 260.5 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), ulcer (What is ulcer?), blood pressure (What is blood pressure?) and. Arava dosage: . During the same period patient was treated with HUMIRA (View Humira Review and Humira Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), CAPTOPRIL (View Captopril Review and Captopril Label ). Patient was hospitalized.

7009247-1 | Abdominal Distension, Abdominal Pain, Ascites, Chromaturia, Decreased Appetite, Encephalopathy, Fatigue, Hepatic Failure, Jaundice
Adverse event was reported on Sep 10, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), hypothyroidism, pain (What is pain?) and. Location: UNITED STATES , weighting 130.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal distension, abdominal pain (What is abdominal pain?), ascites, chromaturia, decreased appetite, encephalopathy, fatigue, hepatic failure, jaundice (What is jaundice?). During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

7004843-X | Dyspnoea, Jaundice, Liver Injury, Oedema
on Sep 15, 2010 Female patient from FRANCE , 60 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient had the following side effects: dyspnoea, jaundice (What is jaundice?), liver injury, oedema. Arava dosage: . Patient was hospitalized.

6992710-7 | Anaemia, Faeces Discoloured, Fatigue, Gingival Bleeding, Impaired Healing, Myalgia, Thrombocytopenia
on Sep 10, 2010 Female patient from MEXICO , 58 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), vitamin supplementation, depression (What is depression?), gastritis and was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: anaemia, faeces discoloured, fatigue, gingival bleeding, impaired healing, myalgia, thrombocytopenia. Arava dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), CALCORT (View Calcort Review and Calcort Label ), SERTRALINE HYDROCHLORIDE (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label ), PRILOSEC (View Prilosec Review and Prilosec Label ). Patient was hospitalized.

6992658-8 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Histiocytosis Haematophagic, Platelet Count Decreased, Rash, Stomatitis, White Blood Cell Count Decreased
Patient was taking Arava (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, histiocytosis haematophagic, platelet count decreased, rash (What is rash?), stomatitis, white blood cell count decreased on Aug 30, 2010 from JAPAN Additional patient health information: Female patient , 51 years of age, weighting 80.47 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), vitamin c deficiency, vitamin supplementation, peripheral circulatory failure and. Arava dosage: . During the same period patient was treated with QUESTRAN (View Questran Review and Questran Label ), PREDNISOLONE (2 Tabletsx2/day) (View Prednisolone Review and Prednisolone Label ), LOXOPROFEN SODIUM (1 Tabletx3/day) (View Loxoprofen Sodium Review and Loxoprofen Sodium Label ), HICEE (1packagex3/day) (View Hicee Review and Hicee Label ), TOCOPHERYL NICOTINATE (1capsulesx3/day) (View Tocopheryl Nicotinate Review and Tocopheryl Nicotinate Label ).

6984726-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased
Adverse event was reported on Sep 14, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), hypertension and. Location: FINLAND , 62 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased. During the same period patient was treated with LESCOL (View Lescol Review and Lescol Label ), LOGIMAX (View Logimax Review and Logimax Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

6978324-3 | Breast Cancer
on Sep 06, 2010 Female patient from AUSTRALIA , 58 years of age, weighting 143.3 lb, was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: breast cancer (What is breast cancer?). Arava dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

6977111-X | Colitis Ulcerative, Diarrhoea
on Sep 08, 2010 Female patient from GERMANY , 32 years of age, was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: colitis ulcerative, diarrhoea. Arava dosage: .

6977067-X | Colon Cancer
Patient was taking Arava (View Usage). Patient had the following side effects: colon cancer on Sep 01, 2010 from AUSTRIA Additional patient health information: Female patient , 57 years of age, weighting 132.3 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with HUMIRA (View Humira Review and Humira Label ), PANTOPRAZOLE (View Pantoprazole Review and Pantoprazole Label ), REMICADE (View Remicade Review and Remicade Label ), SALAZOPYRIN (View Salazopyrin Review and Salazopyrin Label ), VOLTAREN (View Voltaren Review and Voltaren Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6964994-2 | Ascites, Cardiac Failure, Hepatic Cirrhosis, Pericardial Effusion
Adverse event was reported on Aug 27, 2010 by a Male patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: GERMANY , 63 years of age, weighting 158.7 lb, After Arava was administered, patient had the following side effects: ascites, cardiac failure, hepatic cirrhosis, pericardial effusion. During the same period patient was treated with HYALURONATE SODIUM (View Hyaluronate Sodium Review and Hyaluronate Sodium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ). Patient was hospitalized.

6964990-5 | Cardiac Failure, Cardiomyopathy
on Aug 27, 2010 Female patient from SWEDEN , 51 years of age, was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, cardiomyopathy (What is cardiomyopathy?). Arava dosage: . During the same period patient was treated with PLAQUENIL (View Plaquenil Review and Plaquenil Label ), RELIFEX (View Relifex Review and Relifex Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), TIPAROL (View Tiparol Review and Tiparol Label ). Patient was hospitalized.

6960175-7 | Gastrooesophageal Reflux Disease, Skin Cancer
on Aug 23, 2010 Female patient from AUSTRALIA , 71 years of age, was treated with Arava (View Usage). Patient had the following side effects: gastrooesophageal reflux disease, skin cancer (What is skin cancer?). Arava dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

6957518-7 | Colitis, Diarrhoea, Eosinophil Count Increased, Gastrointestinal Haemorrhage, Histiocytosis Haematophagic, Liver Injury, Lung Infection, Multi-organ Failure
Patient was taking Arava (View Usage). After Arava was administered, patient had the following side effects: colitis, diarrhoea, eosinophil count increased, gastrointestinal haemorrhage, histiocytosis haematophagic, liver injury, lung infection, multi-organ failure on Aug 25, 2010 from FRANCE Additional patient health information: Female patient , 64 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with APRANAX (View Apranax Review and Apranax Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), PRETERAX (View Preterax Review and Preterax Label ), NAPROSYN (View Naprosyn Review and Naprosyn Label ). Patient was hospitalized.

6945612-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased
Adverse event was reported on Aug 20, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: POLAND , 41 years of age, weighting 167.6 lb, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased. During the same period patient was treated with METHOTREXATE SODIUM (View Methotrexate Sodium Review and Methotrexate Sodium Label ), METHYLPREDNISOLONE (View Methylprednisolone Review and Methylprednisolone Label ), SORBIFER DURULES (View Sorbifer Durules Review and Sorbifer Durules Label ), DETRALEX (View Detralex Review and Detralex Label ).

6945603-5 | Deep Vein Thrombosis, Pulmonary Embolism
on Aug 19, 2010 Female patient from BRAZIL , 56 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), fibromyalgia and was treated with Arava (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), pulmonary embolism (What is pulmonary embolism?). Arava dosage: . During the same period patient was treated with ADALIMUMAB (View Adalimumab Review and Adalimumab Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), DIACEREIN (View Diacerein Review and Diacerein Label ). Patient was hospitalized.

6941279-1 | Liver Function Test Abnormal
on Aug 18, 2010 Female patient from CZECH REPUBLIC , 53 years of age, weighting 131.2 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: liver function test abnormal. Arava dosage: . During the same period patient was treated with LESCOL XL (View Lescol Xl Review and Lescol Xl Label ), HELICID (View Helicid Review and Helicid Label ), ESSENTIALE FORTE (View Essentiale Forte Review and Essentiale Forte Label ), SILYMARIN (View Silymarin Review and Silymarin Label ), MELOXICAM (View Meloxicam Review and Meloxicam Label ), PREDNISONE (View Prednisone Review and Prednisone Label ).

6938286-1 | Cataract
Patient was taking Arava (View Usage). Patient experienced the following unwanted or unexpected effects: cataract (What is cataract?) on Aug 16, 2010 from AUSTRALIA Additional patient health information: Female patient , 51 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), ACETAMINOPHEN W/ CODEINE (View Acetaminophen W/ Codeine Review and Acetaminophen W/ Codeine Label ).

6938285-X | Cerebral Vasoconstriction
Adverse event was reported on Aug 16, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) . Location: SPAIN , 50 years of age, Patient had the following side effects: cerebral vasoconstriction. Patient was hospitalized.

6931647-6 | Asthenia, Fear, Hyperaemia, Hypertensive Crisis, Hypoaesthesia
on Aug 05, 2010 Female patient from RUSSIAN FEDERATION , 67 years of age, was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: asthenia, fear, hyperaemia, hypertensive crisis, hypoaesthesia. Arava dosage: . During the same period patient was treated with METHYLPREDNISOLONE (View Methylprednisolone Review and Methylprednisolone Label ). Patient was hospitalized.

6931086-8 | Pancytopenia
on Aug 17, 2010 Female patient from UNITED STATES , 86 years of age, weighting 133.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: pancytopenia. Arava dosage: 5 Times A Week Po. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), BONIVA (View Boniva Review and Boniva Label ), UNIRETIC (View Uniretic Review and Uniretic Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), KLOR CON (View Klor-con Review and Klor-con Label ), CALCIUM + VIT D (View Calcium + Vit D Review and Calcium + Vit D Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ). Patient was hospitalized.

6929750-X | Lung Neoplasm Malignant
Patient was taking Arava (View Usage). Patient had the following side effects: lung neoplasm malignant on Aug 12, 2010 from FRANCE Additional patient health information: Male patient , 64 years of age, . Arava dosage: . During the same period patient was treated with REMICADE (View Remicade Review and Remicade Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), KINERET (View Kineret Review and Kineret Label ), HUMIRA (View Humira Review and Humira Label ), ETANERCEPT (View Etanercept Review and Etanercept Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ), MABTHERA (View Mabthera Review and Mabthera Label ). Patient was hospitalized.

6929738-9 | Abscess Limb, Arthralgia, Arthritis, Red Blood Cell Sedimentation Rate Increased, Renal Failure Chronic
Adverse event was reported on Aug 10, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), vasculitis (What is vasculitis?) and. Location: UNITED STATES , 45 years of age, After Arava was administered, patient had the following side effects: abscess limb, arthralgia, arthritis (What is arthritis?), red blood cell sedimentation rate increased, renal failure chronic. During the same period patient was treated with ETANERCEPT (View Etanercept Review and Etanercept Label ), IMURAN (View Imuran Review and Imuran Label ), CELLCEPT (View Cellcept Review and Cellcept Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), ACYCLOVIR (View Acyclovir Review and Acyclovir Label ).

6929733-X | Renal Failure
on Aug 05, 2010 Female patient from AUSTRALIA , 73 years of age, was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure. Arava dosage: . During the same period patient was treated with FISH OIL (View Fish Oil Review and Fish Oil Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), MONODUR (View Monodur Review and Monodur Label ).

6924917-9 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Pruritus
on Aug 12, 2010 Female patient from JAPAN , 57 years of age, weighting 121.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), gastritis prophylaxis, hypertension, vitamin supplementation and was treated with Arava (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, pruritus. Arava dosage: . During the same period patient was treated with QUESTRAN (View Questran Review and Questran Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), HYDROCHLOROTHIAZIDE/LOSARTAN POTASSIUM (View Hydrochlorothiazide/losartan Potassium Review and Hydrochlorothiazide/losartan Potassium Label ), CINAL (View Cinal Review and Cinal Label ), HYTHIOL (View Hythiol Review and Hythiol Label ). Patient was hospitalized.

6922530-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased
Patient was taking Arava (View Usage). After Arava was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased on Aug 03, 2010 from FINLAND Additional patient health information: Female patient , 62 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), hypertension and. Arava dosage: . During the same period patient was treated with LESCOL (View Lescol Review and Lescol Label ), LOGIMAX (View Logimax Review and Logimax Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

6916570-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased
Adverse event was reported on Aug 03, 2010 by a Female patient taking Arava (View Usage) (Dosage: ) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), hypertension and. Location: FINLAND , 62 years of age, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased. During the same period patient was treated with LESCOL (View Lescol Review and Lescol Label ), LOGIMAX (View Logimax Review and Logimax Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

6910807-4 | Acute Coronary Syndrome, Myocardial Infarction
on Jul 06, 2010 Female patient from FRANCE , 55 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). Patient had the following side effects: acute coronary syndrome, myocardial infarction. Arava dosage: . During the same period patient was treated with ETANERCEPT (1 Dosage Form Once A Week) (View Etanercept Review and Etanercept Label ). Patient was hospitalized.

6907781-3 | Hepatitis Toxic
on Aug 03, 2010 Male patient from GERMANY , 63 years of age, weighting 196.2 lb, was diagnosed with diabetes mellitus and was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: hepatitis toxic. Arava dosage: . During the same period patient was treated with PANTOPRAZOLE (View Pantoprazole Review and Pantoprazole Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), ORAL ANTIDIABETICS (View Oral Antidiabetics Review and Oral Antidiabetics Label ), RAMIPRIL (Daily Dose: 5 Mg Millgram(s) Every Days) (View Ramipril Review and Ramipril Label ), DECORTIN H (Daily Dose: 1 Df Dosage Form Every Days) (View Decortin-h Review and Decortin-h Label ), MTX (Daily Dose: 20 Mg Millgram(s) Every Weeks) (View Mtx Review and Mtx Label ), NOVAMIN (View Novamin Review and Novamin Label ), FOLSAN (15/week) (View Folsan Review and Folsan Label ).

6905387-3 | Acute Pulmonary Oedema, Lung Disorder, Pulmonary Hypertensive Crisis
Patient was taking Arava (View Usage). Patient experienced the following unwanted or unexpected effects: acute pulmonary oedema, lung disorder, pulmonary hypertensive crisis on Jul 26, 2010 from FRANCE Additional patient health information: Male patient , 57 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with CORTANCYL (View Cortancyl Review and Cortancyl Label ), ORENCIA (View Orencia Review and Orencia Label ). Patient was hospitalized.

6899876-8 | Alopecia, Collapse Of Lung, Dyspnoea, Erectile Dysfunction, Hot Flush, Pneumonia
Adverse event was reported on Jul 22, 2010 by a Male patient taking Arava (View Usage) (Dosage: 20 Milligram(s)) was diagnosed with arthritis (What is arthritis?) and. Location: DENMARK , 55 years of age, weighting 282.2 lb, Patient had the following side effects: alopecia, collapse of lung, dyspnoea, erectile dysfunction (What is erectile dysfunction?), hot flush, pneumonia (What is pneumonia?). Patient was hospitalized.

6894329-5 | Brain Oedema, Diplopia, Dizziness, Hallucination, Hallucination, Auditory, Leukoencephalopathy
on Jul 20, 2010 Male patient from JAPAN , 52 years of age, weighting 121.3 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Arava (View Usage). After Arava was administered, patient had the following side effects: brain oedema, diplopia, dizziness (What is dizziness?), hallucination, hallucination, auditory, leukoencephalopathy. Arava dosage: . During the same period patient was treated with ETANERCEPT (View Etanercept Review and Etanercept Label ), MEDROL (View Medrol Review and Medrol Label ), QUESTRAN (View Questran Review and Questran Label ). Patient was hospitalized.

6879741-2 | Bowen's Disease, Gingivitis
on Jul 16, 2010 Male patient from AUSTRALIA , 79 years of age, was treated with Arava (View Usage). Patient experienced the following unwanted or unexpected effects: bowen's disease, gingivitis. Arava dosage: . During the same period patient was treated with ADVANTAN (View Advantan Review and Advantan Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), LOPERAMIDE (View Loperamide Review and Loperamide Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PANAMAX (View Panamax Review and Panamax Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

6879733-3 | Breast Cancer, Primary Mediastinal Large B-cell Lymphoma Recurrent
Patient was taking Arava (View Usage). Patient had the following side effects: breast cancer (What is breast cancer?), primary mediastinal large b-cell lymphoma recurrent on Jul 06, 2010 from FRANCE Additional patient health information: Female patient , 58 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Arava dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), REMICADE (View Remicade Review and Remicade Label ), ENBREL (View Enbrel Review and Enbrel Label ), HUMIRA (View Humira Review and Humira Label ), MABTHERA (View Mabthera Review and Mabthera Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), ACECLOFENAC (View Aceclofenac Review and Aceclofenac Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ).