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

AGGRESSION ( 15 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
OVERDOSE ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
DEPRESSION ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
PSYCHOTIC DISORDER ( 9 FDA reports)
DIZZINESS ( 8 FDA reports)
ANGER ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
CHEST PAIN ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PARANOIA ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
HALLUCINATION ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
MANIA ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
PAIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TIC ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACNE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL PAIN MALE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STARING ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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