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

ANAEMIA ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
INJECTION SITE ULCER ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
ENDOTOXIC SHOCK ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RASH ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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