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

ANAEMIA ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PAIN ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)

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