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

VOMITING ( 7 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
HYPOXIA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
RENAL HAEMORRHAGE ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
GASTROENTERITIS RADIATION ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HEADACHE ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
INFECTION ( 1 FDA reports)

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