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

SEPSIS ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
ASTHMA ( 6 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CHOKING ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)

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