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OESOPHAGEAL CANDIDIASIS ( 9 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
VOMITING ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)

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