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MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 4 FDA reports)
LATENT TUBERCULOSIS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
PNEUMONIA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
VULVAL CANCER STAGE 0 ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
FALL ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)

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