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

ANAEMIA ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
PRURITUS ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
FALL ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CORNEAL HYPERTROPHY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERPANGINA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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