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

VOMITING ( 6 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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