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

DEPRESSION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
MANIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
IRITIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)

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