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

DRUG INTERACTION ( 23 FDA reports)
CONVULSION ( 11 FDA reports)
MALAISE ( 11 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
VOMITING ( 9 FDA reports)
NAUSEA ( 8 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
MYOCLONIC EPILEPSY ( 5 FDA reports)
SEROTONIN SYNDROME ( 5 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
APATHY ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
MELAENA ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
THIRST ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URETHRAL NEOPLASM ( 2 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SOPOR ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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