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

GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
INSOMNIA ( 5 FDA reports)
DYSGEUSIA ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
COMA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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