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

OVERDOSE ( 7 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
AGITATION ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
MOANING ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
AUTISM SPECTRUM DISORDER ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
POISONING ( 3 FDA reports)
SEDATION ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ATELECTASIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAST-POINTING ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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