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

MALAISE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ABASIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
CRYING ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
APATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VISCERAL LEISHMANIASIS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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