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

DRUG INTERACTION ( 4 FDA reports)
AGITATION ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
FALL ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINITIS GARDNERELLA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
WOUND ( 1 FDA reports)

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