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

GASTROENTERITIS ( 27 FDA reports)
DEPRESSION ( 24 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 24 FDA reports)
SUICIDAL IDEATION ( 23 FDA reports)
INSOMNIA ( 19 FDA reports)
VOMITING ( 18 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 17 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 15 FDA reports)
ABNORMAL BEHAVIOUR ( 13 FDA reports)
APPENDICITIS ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
SELF ESTEEM DECREASED ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
AGGRESSION ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
IRRITABILITY ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
DIABETIC KETOACIDOSIS ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
CONVULSION ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
THYROID MASS ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
PALLOR ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ANGER ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
COUGH ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
FALL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AUTISM SPECTRUM DISORDER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELAYED PUBERTY ( 2 FDA reports)
DENGUE FEVER ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYDENHAM'S CHOREA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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