Please choose an event type to view the corresponding MedsFacts report:

DEATH ( 7 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLISTER ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
INJURY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
PAIN ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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