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

RASH ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PAIN ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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