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

DRY MOUTH ( 6 FDA reports)
HYPOTENSION ( 4 FDA reports)
VASOSPASM ( 2 FDA reports)
RASH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DEATH ( 2 FDA reports)
CONVULSION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MESENTERIC ATHEROSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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