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

LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
SEDATION ( 8 FDA reports)
GLAUCOMA ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
AGGRESSION ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
TIC ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
MANIA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FALL ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
ANOREXIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
CRYING ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RASH ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
TREMOR ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJURY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)

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