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

COMPLETED SUICIDE ( 65 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 46 FDA reports)
DRUG TOXICITY ( 38 FDA reports)
DRUG ABUSE ( 34 FDA reports)
CARDIAC ARREST ( 29 FDA reports)
DRUG INTERACTION ( 29 FDA reports)
DIZZINESS ( 25 FDA reports)
RESPIRATORY ARREST ( 25 FDA reports)
OVERDOSE ( 24 FDA reports)
DEATH ( 23 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
DYSPNOEA ( 18 FDA reports)
HEADACHE ( 17 FDA reports)
PULMONARY OEDEMA ( 16 FDA reports)
ANXIETY ( 15 FDA reports)
FALL ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
AGITATION ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
INTENTIONAL DRUG MISUSE ( 13 FDA reports)
HEART RATE INCREASED ( 12 FDA reports)
MULTIPLE DRUG OVERDOSE ( 12 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 12 FDA reports)
POISONING ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
CHEST PAIN ( 11 FDA reports)
DEPRESSION ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 11 FDA reports)
AGGRESSION ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 9 FDA reports)
COMA ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
PAIN ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
THROAT TIGHTNESS ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
DRUG ABUSER ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SUBSTANCE ABUSE ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ACCIDENTAL DEATH ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 7 FDA reports)
INJURY ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
CONCUSSION ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DEVELOPMENTAL DELAY ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
MANIA ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ALCOHOL USE ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
POLYSUBSTANCE ABUSE ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
RASH ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
STRESS ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACCIDENTAL POISONING ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FEAR ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MENOPAUSE ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
CARDITIS ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONGENITAL NYSTAGMUS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SYDENHAM'S CHOREA ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISION ABNORMAL NEONATAL ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APATHY ( 1 FDA reports)
APNOEA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
AURA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DURAL FISTULA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOTONY OF EYE ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TIC ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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