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

PLATELET COUNT DECREASED ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
CRYING ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
COUGH ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STARING ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use