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

VOMITING ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
OVERDOSE ( 5 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
SOCIAL PHOBIA ( 4 FDA reports)
SEPSIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
AGITATION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)

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