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

SEPSIS ( 10 FDA reports)
ASTHENIA ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
DEATH ( 6 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
PRURITUS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
INFECTION ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
RASH ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
HIV INFECTION CDC CATEGORY C2 ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
COUGH ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)

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