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

DYSPNOEA ( 7 FDA reports)
PNEUMONIA ( 6 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
RASH ( 3 FDA reports)
WHEEZING ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
ANTI FACTOR X ANTIBODY POSITIVE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)

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