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

COLITIS ( 8 FDA reports)
NAUSEA ( 7 FDA reports)
PNEUMONIA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
FATIGUE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
COUGH ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)

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