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

VOMITING ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)

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