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

DIZZINESS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
VOMITING ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BILE DUCT NECROSIS ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
GASTRIC ULCER HELICOBACTER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INFECTION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
TENSION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NECROTISING PANNICULITIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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