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RHEUMATOID ARTHRITIS ( 8 FDA reports)
BACTERAEMIA ( 6 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
LUMBAR SPINAL STENOSIS ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
HERPES ZOSTER OTICUS ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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