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CONDITION AGGRAVATED ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
SYNCOPE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
APATHY ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
DEMENTIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)

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