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

SOMNOLENCE ( 5 FDA reports)
DIZZINESS ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
AMIMIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ABASIA ( 2 FDA reports)
FALL ( 2 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DROWNING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SEDATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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