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

STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
DEHYDRATION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
FALL ( 5 FDA reports)
INJURY ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
FLUID REPLACEMENT ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)

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