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

VOMITING ( 31 FDA reports)
AGGRESSION ( 26 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 18 FDA reports)
MYOCARDIAL INFARCTION ( 18 FDA reports)
RASH ( 18 FDA reports)
ABNORMAL BEHAVIOUR ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
TIC ( 16 FDA reports)
APPENDICITIS ( 15 FDA reports)
INFECTION ( 15 FDA reports)
WEIGHT INCREASED ( 15 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
IRRITABILITY ( 13 FDA reports)
AGITATION ( 12 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
VITH NERVE PARALYSIS ( 12 FDA reports)
IMPULSIVE BEHAVIOUR ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
SUICIDE ATTEMPT ( 11 FDA reports)
THYROIDITIS ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
PYREXIA ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CRYING ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 9 FDA reports)
AFFECT LABILITY ( 8 FDA reports)
ALCOHOL ABUSE ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 8 FDA reports)
LEARNING DISABILITY ( 8 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
RESTLESSNESS ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HYPERTHYROIDISM ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
APATHY ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
FALL ( 6 FDA reports)
LEARNING DISORDER ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TREMOR ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
ASPIRATION ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
ENURESIS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
COUGH ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATITIS ALCOHOLIC ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
MANIA ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SYDENHAM'S CHOREA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANGER ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
AUTISM SPECTRUM DISORDER ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHOKING ( 3 FDA reports)
DEATH ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THOUGHT BROADCASTING ( 3 FDA reports)
TOURETTE'S DISORDER ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FOETAL ACIDOSIS ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TENSION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
ACNE ( 1 FDA reports)
ALLERGIC COUGH ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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