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

SUICIDE ATTEMPT ( 747 FDA reports)
OVERDOSE ( 617 FDA reports)
INTENTIONAL OVERDOSE ( 502 FDA reports)
AGGRESSION ( 342 FDA reports)
SOMNOLENCE ( 336 FDA reports)
LOSS OF CONSCIOUSNESS ( 334 FDA reports)
VOMITING ( 333 FDA reports)
DRUG INTERACTION ( 318 FDA reports)
ALCOHOL USE ( 308 FDA reports)
AMNESIA ( 304 FDA reports)
SUICIDAL IDEATION ( 288 FDA reports)
NAUSEA ( 270 FDA reports)
COMPLETED SUICIDE ( 261 FDA reports)
ALCOHOL POISONING ( 253 FDA reports)
DEPRESSION ( 251 FDA reports)
AGITATION ( 226 FDA reports)
ALCOHOL INTERACTION ( 225 FDA reports)
ROAD TRAFFIC ACCIDENT ( 218 FDA reports)
CONVULSION ( 213 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 213 FDA reports)
ANXIETY ( 209 FDA reports)
TACHYCARDIA ( 203 FDA reports)
DRUG TOXICITY ( 179 FDA reports)
DIZZINESS ( 177 FDA reports)
COMA ( 176 FDA reports)
FATIGUE ( 176 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 168 FDA reports)
INSOMNIA ( 165 FDA reports)
ABNORMAL BEHAVIOUR ( 162 FDA reports)
CONFUSIONAL STATE ( 162 FDA reports)
SUBSTANCE ABUSE ( 160 FDA reports)
ASTHENIA ( 154 FDA reports)
MULTIPLE DRUG OVERDOSE ( 154 FDA reports)
MALAISE ( 153 FDA reports)
HEADACHE ( 151 FDA reports)
HYPOTENSION ( 151 FDA reports)
DEATH ( 147 FDA reports)
FALL ( 146 FDA reports)
FEELING ABNORMAL ( 136 FDA reports)
TREMOR ( 131 FDA reports)
DIARRHOEA ( 122 FDA reports)
HYPERHIDROSIS ( 120 FDA reports)
DRUG ABUSE ( 115 FDA reports)
HALLUCINATION ( 115 FDA reports)
BLOOD ALCOHOL INCREASED ( 113 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 110 FDA reports)
DYSARTHRIA ( 110 FDA reports)
MEMORY IMPAIRMENT ( 109 FDA reports)
DRUG INEFFECTIVE ( 108 FDA reports)
PAIN ( 108 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 105 FDA reports)
CARDIAC ARREST ( 104 FDA reports)
INTENTIONAL DRUG MISUSE ( 104 FDA reports)
SOMNAMBULISM ( 104 FDA reports)
DYSPNOEA ( 102 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 101 FDA reports)
WEIGHT DECREASED ( 101 FDA reports)
IMPAIRED DRIVING ABILITY ( 97 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 95 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 94 FDA reports)
DRUG DEPENDENCE ( 94 FDA reports)
PSYCHOTIC DISORDER ( 92 FDA reports)
HYPERTENSION ( 87 FDA reports)
GRAND MAL CONVULSION ( 84 FDA reports)
ABDOMINAL PAIN ( 83 FDA reports)
ALCOHOL ABUSE ( 83 FDA reports)
HEPATIC ENZYME INCREASED ( 82 FDA reports)
PYREXIA ( 81 FDA reports)
NIGHTMARE ( 79 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 78 FDA reports)
IRRITABILITY ( 78 FDA reports)
ALCOHOLISM ( 76 FDA reports)
RESTLESSNESS ( 76 FDA reports)
RENAL FAILURE ACUTE ( 73 FDA reports)
ANGER ( 72 FDA reports)
DISORIENTATION ( 70 FDA reports)
PHYSICAL ASSAULT ( 70 FDA reports)
DISTURBANCE IN ATTENTION ( 68 FDA reports)
RHABDOMYOLYSIS ( 68 FDA reports)
MOOD SWINGS ( 66 FDA reports)
DEPRESSED MOOD ( 65 FDA reports)
DRUG ABUSER ( 64 FDA reports)
HEPATIC FAILURE ( 64 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 63 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 63 FDA reports)
GAIT DISTURBANCE ( 63 FDA reports)
ILL-DEFINED DISORDER ( 63 FDA reports)
INTENTIONAL MISUSE ( 63 FDA reports)
POISONING ( 63 FDA reports)
TREATMENT NONCOMPLIANCE ( 63 FDA reports)
CONSTIPATION ( 62 FDA reports)
INTENTIONAL SELF-INJURY ( 62 FDA reports)
PARAESTHESIA ( 62 FDA reports)
BLOOD BILIRUBIN INCREASED ( 61 FDA reports)
PARANOIA ( 61 FDA reports)
SINUS TACHYCARDIA ( 60 FDA reports)
ABNORMAL DREAMS ( 59 FDA reports)
BALANCE DISORDER ( 58 FDA reports)
LETHARGY ( 58 FDA reports)
VISION BLURRED ( 58 FDA reports)
DECREASED APPETITE ( 55 FDA reports)
METABOLIC ACIDOSIS ( 55 FDA reports)
RESPIRATORY FAILURE ( 55 FDA reports)
SYNCOPE ( 55 FDA reports)
WEIGHT INCREASED ( 55 FDA reports)
HEAD INJURY ( 54 FDA reports)
CRYING ( 53 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 53 FDA reports)
DELIRIUM ( 52 FDA reports)
UNRESPONSIVE TO STIMULI ( 52 FDA reports)
DEHYDRATION ( 51 FDA reports)
SOPOR ( 51 FDA reports)
ABDOMINAL PAIN UPPER ( 50 FDA reports)
CHEST PAIN ( 50 FDA reports)
MANIA ( 50 FDA reports)
MYDRIASIS ( 50 FDA reports)
OFF LABEL USE ( 50 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 49 FDA reports)
HOMICIDAL IDEATION ( 49 FDA reports)
HYPOAESTHESIA ( 49 FDA reports)
HYPOGLYCAEMIA ( 49 FDA reports)
HYPOKALAEMIA ( 49 FDA reports)
PANIC ATTACK ( 49 FDA reports)
SLEEP WALKING ( 49 FDA reports)
HOMICIDE ( 48 FDA reports)
INJURY ( 46 FDA reports)
DRUG LEVEL INCREASED ( 45 FDA reports)
EUPHORIC MOOD ( 45 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 45 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 44 FDA reports)
HEPATITIS ( 44 FDA reports)
RENAL FAILURE ( 44 FDA reports)
ANAEMIA ( 43 FDA reports)
MUSCLE SPASMS ( 43 FDA reports)
HEART RATE INCREASED ( 42 FDA reports)
MYOCARDIAL INFARCTION ( 42 FDA reports)
PRURITUS ( 42 FDA reports)
ACCIDENTAL OVERDOSE ( 41 FDA reports)
HEPATOMEGALY ( 41 FDA reports)
INFLUENZA LIKE ILLNESS ( 41 FDA reports)
PNEUMONIA ( 41 FDA reports)
PALPITATIONS ( 40 FDA reports)
SLEEP DISORDER ( 40 FDA reports)
BACK PAIN ( 39 FDA reports)
CYANOSIS ( 39 FDA reports)
INCORRECT DOSE ADMINISTERED ( 39 FDA reports)
MENTAL STATUS CHANGES ( 39 FDA reports)
WITHDRAWAL SYNDROME ( 39 FDA reports)
BLOOD PRESSURE INCREASED ( 38 FDA reports)
CONDITION AGGRAVATED ( 38 FDA reports)
MYALGIA ( 38 FDA reports)
AKATHISIA ( 37 FDA reports)
ANOREXIA ( 37 FDA reports)
ASPIRATION ( 37 FDA reports)
EMOTIONAL DISORDER ( 37 FDA reports)
PAIN IN EXTREMITY ( 37 FDA reports)
PERSONALITY CHANGE ( 37 FDA reports)
PNEUMONIA ASPIRATION ( 37 FDA reports)
BLOOD PRESSURE DECREASED ( 36 FDA reports)
CIRCULATORY COLLAPSE ( 36 FDA reports)
NERVOUSNESS ( 36 FDA reports)
NYSTAGMUS ( 36 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 36 FDA reports)
BLOOD CREATININE INCREASED ( 35 FDA reports)
RESPIRATORY ARREST ( 35 FDA reports)
RESPIRATORY DEPRESSION ( 35 FDA reports)
TEARFULNESS ( 35 FDA reports)
CONTUSION ( 34 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 34 FDA reports)
LACTIC ACIDOSIS ( 34 FDA reports)
LIVER INJURY ( 34 FDA reports)
OEDEMA PERIPHERAL ( 34 FDA reports)
RASH ( 34 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 33 FDA reports)
ARTHRALGIA ( 33 FDA reports)
DRUG SCREEN POSITIVE ( 33 FDA reports)
GUN SHOT WOUND ( 33 FDA reports)
HYPOXIA ( 33 FDA reports)
PULMONARY OEDEMA ( 33 FDA reports)
HEPATIC STEATOSIS ( 32 FDA reports)
MIOSIS ( 32 FDA reports)
SPEECH DISORDER ( 32 FDA reports)
DELUSION ( 31 FDA reports)
FEAR ( 31 FDA reports)
SWELLING FACE ( 31 FDA reports)
ABDOMINAL DISCOMFORT ( 30 FDA reports)
BIPOLAR DISORDER ( 30 FDA reports)
HEPATIC CIRRHOSIS ( 30 FDA reports)
HYPONATRAEMIA ( 30 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 30 FDA reports)
MULTI-ORGAN FAILURE ( 30 FDA reports)
SEROTONIN SYNDROME ( 30 FDA reports)
BLOOD POTASSIUM DECREASED ( 29 FDA reports)
HEPATOTOXICITY ( 29 FDA reports)
LIBIDO DECREASED ( 29 FDA reports)
MENTAL DISORDER ( 29 FDA reports)
DRY MOUTH ( 28 FDA reports)
HALLUCINATION, VISUAL ( 28 FDA reports)
HYPERSENSITIVITY ( 28 FDA reports)
JAUNDICE ( 28 FDA reports)
SUICIDAL BEHAVIOUR ( 28 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 28 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 27 FDA reports)
BRADYCARDIA ( 27 FDA reports)
PERSONALITY DISORDER ( 27 FDA reports)
SEDATION ( 27 FDA reports)
ACUTE HEPATIC FAILURE ( 26 FDA reports)
ARRHYTHMIA ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 26 FDA reports)
DIABETES MELLITUS ( 26 FDA reports)
FLATULENCE ( 26 FDA reports)
FLUSHING ( 26 FDA reports)
SHOCK ( 26 FDA reports)
THINKING ABNORMAL ( 26 FDA reports)
ACCIDENTAL DEATH ( 25 FDA reports)
APATHY ( 25 FDA reports)
BRAIN OEDEMA ( 25 FDA reports)
COORDINATION ABNORMAL ( 25 FDA reports)
DYSPHAGIA ( 25 FDA reports)
ENCEPHALOPATHY ( 25 FDA reports)
LIVER DISORDER ( 25 FDA reports)
MEDICATION ERROR ( 25 FDA reports)
SKIN LACERATION ( 25 FDA reports)
TACHYPNOEA ( 25 FDA reports)
ABDOMINAL DISTENSION ( 24 FDA reports)
ATAXIA ( 24 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 24 FDA reports)
CHROMATURIA ( 24 FDA reports)
EATING DISORDER ( 24 FDA reports)
GASTRITIS ( 24 FDA reports)
HAEMATEMESIS ( 24 FDA reports)
HAEMORRHAGE ( 24 FDA reports)
HALLUCINATION, AUDITORY ( 24 FDA reports)
PERIPHERAL COLDNESS ( 24 FDA reports)
STRESS ( 24 FDA reports)
VERTIGO ( 24 FDA reports)
ALCOHOL INTOLERANCE ( 23 FDA reports)
ASCITES ( 23 FDA reports)
COGNITIVE DISORDER ( 23 FDA reports)
DYSPEPSIA ( 23 FDA reports)
LACERATION ( 23 FDA reports)
PALLOR ( 23 FDA reports)
VENTRICULAR TACHYCARDIA ( 23 FDA reports)
VISUAL ACUITY REDUCED ( 23 FDA reports)
DISINHIBITION ( 22 FDA reports)
FAECES DISCOLOURED ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 22 FDA reports)
MOOD ALTERED ( 22 FDA reports)
SELF-INJURIOUS IDEATION ( 22 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 21 FDA reports)
CEREBROVASCULAR ACCIDENT ( 21 FDA reports)
CONCUSSION ( 21 FDA reports)
DEPENDENCE ( 21 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
HYPERSOMNIA ( 21 FDA reports)
IMPRISONMENT ( 21 FDA reports)
MAJOR DEPRESSION ( 21 FDA reports)
OCULAR HYPERAEMIA ( 21 FDA reports)
PREMATURE BABY ( 21 FDA reports)
SLEEP TALKING ( 21 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 21 FDA reports)
ASPHYXIA ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 20 FDA reports)
FEELING DRUNK ( 20 FDA reports)
MENTAL IMPAIRMENT ( 20 FDA reports)
MUSCULAR WEAKNESS ( 20 FDA reports)
PANCREATITIS ( 20 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
VENTRICULAR FIBRILLATION ( 20 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 19 FDA reports)
ACIDOSIS ( 19 FDA reports)
CARDIAC DISORDER ( 19 FDA reports)
CORONARY ARTERY DISEASE ( 19 FDA reports)
IMPULSIVE BEHAVIOUR ( 19 FDA reports)
PULMONARY CONGESTION ( 19 FDA reports)
SEXUAL DYSFUNCTION ( 19 FDA reports)
URINARY TRACT INFECTION ( 19 FDA reports)
APNOEA ( 18 FDA reports)
CHEST DISCOMFORT ( 18 FDA reports)
DEVELOPMENTAL DELAY ( 18 FDA reports)
DRUG EFFECT DECREASED ( 18 FDA reports)
ERECTILE DYSFUNCTION ( 18 FDA reports)
LEGAL PROBLEM ( 18 FDA reports)
RASH ERYTHEMATOUS ( 18 FDA reports)
SELF-MEDICATION ( 18 FDA reports)
SLUGGISHNESS ( 18 FDA reports)
TOOTH DISORDER ( 18 FDA reports)
TRANSAMINASES INCREASED ( 18 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 17 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 17 FDA reports)
AFFECTIVE DISORDER ( 17 FDA reports)
ANURIA ( 17 FDA reports)
CEREBELLAR SYNDROME ( 17 FDA reports)
HOSTILITY ( 17 FDA reports)
HYPERLIPIDAEMIA ( 17 FDA reports)
HYPOTHERMIA ( 17 FDA reports)
MEAN CELL VOLUME INCREASED ( 17 FDA reports)
MELAENA ( 17 FDA reports)
NERVOUS SYSTEM DISORDER ( 17 FDA reports)
PLEURAL EFFUSION ( 17 FDA reports)
PREGNANCY ( 17 FDA reports)
SEXUAL ABUSE ( 17 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 17 FDA reports)
ABSCESS ( 16 FDA reports)
AFFECT LABILITY ( 16 FDA reports)
BLOOD UREA INCREASED ( 16 FDA reports)
CELLULITIS ( 16 FDA reports)
DISSOCIATION ( 16 FDA reports)
EPILEPSY ( 16 FDA reports)
FEELING OF DESPAIR ( 16 FDA reports)
HEPATIC NECROSIS ( 16 FDA reports)
HYPERGLYCAEMIA ( 16 FDA reports)
LOWER LIMB FRACTURE ( 16 FDA reports)
MUSCLE TWITCHING ( 16 FDA reports)
MYOCLONUS ( 16 FDA reports)
PROTHROMBIN TIME PROLONGED ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
RENAL TUBULAR NECROSIS ( 16 FDA reports)
RESPIRATORY RATE INCREASED ( 16 FDA reports)
SCHIZOPHRENIA ( 16 FDA reports)
SELF MUTILATION ( 16 FDA reports)
THEFT ( 16 FDA reports)
BLOOD GLUCOSE DECREASED ( 15 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 15 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 15 FDA reports)
CARDIOMEGALY ( 15 FDA reports)
CHILLS ( 15 FDA reports)
DRUG DIVERSION ( 15 FDA reports)
EMOTIONAL DISTRESS ( 15 FDA reports)
ERYTHEMA ( 15 FDA reports)
EXCORIATION ( 15 FDA reports)
FACIAL PALSY ( 15 FDA reports)
FLAT AFFECT ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
HEPATIC ENCEPHALOPATHY ( 15 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 15 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 15 FDA reports)
NO ADVERSE EVENT ( 15 FDA reports)
RIB FRACTURE ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 15 FDA reports)
ABASIA ( 14 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
COAGULOPATHY ( 14 FDA reports)
DEREALISATION ( 14 FDA reports)
DYSURIA ( 14 FDA reports)
EJECTION FRACTION DECREASED ( 14 FDA reports)
ELECTRIC SHOCK ( 14 FDA reports)
EPISTAXIS ( 14 FDA reports)
HAEMODIALYSIS ( 14 FDA reports)
HANGOVER ( 14 FDA reports)
HEMIPARESIS ( 14 FDA reports)
HOT FLUSH ( 14 FDA reports)
HYPERCHOLESTEROLAEMIA ( 14 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 14 FDA reports)
MIGRAINE ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
SPINAL COMPRESSION FRACTURE ( 14 FDA reports)
SWELLING ( 14 FDA reports)
TINNITUS ( 14 FDA reports)
VICTIM OF SEXUAL ABUSE ( 14 FDA reports)
ANOXIC ENCEPHALOPATHY ( 13 FDA reports)
ATRIAL SEPTAL DEFECT ( 13 FDA reports)
BLOOD ALBUMIN DECREASED ( 13 FDA reports)
BLOOD SODIUM DECREASED ( 13 FDA reports)
BODY TEMPERATURE DECREASED ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
CARDIOMYOPATHY ( 13 FDA reports)
CONJUNCTIVITIS ( 13 FDA reports)
DECREASED INTEREST ( 13 FDA reports)
DEPERSONALISATION ( 13 FDA reports)
DILATATION VENTRICULAR ( 13 FDA reports)
DRUG HYPERSENSITIVITY ( 13 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 13 FDA reports)
FEELING JITTERY ( 13 FDA reports)
FOOT FRACTURE ( 13 FDA reports)
HEPATITIS C ( 13 FDA reports)
HYPOMANIA ( 13 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
MITRAL VALVE INCOMPETENCE ( 13 FDA reports)
NEUROPATHY PERIPHERAL ( 13 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 13 FDA reports)
RESPIRATORY ACIDOSIS ( 13 FDA reports)
RESPIRATORY DISTRESS ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SOCIAL PHOBIA ( 13 FDA reports)
SPLENOMEGALY ( 13 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 13 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 13 FDA reports)
UNEVALUABLE EVENT ( 13 FDA reports)
VISUAL IMPAIRMENT ( 13 FDA reports)
ABDOMINAL TENDERNESS ( 12 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 12 FDA reports)
ANAEMIA MACROCYTIC ( 12 FDA reports)
ARTHROPOD STING ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
BURNING SENSATION ( 12 FDA reports)
CARDIOPULMONARY FAILURE ( 12 FDA reports)
COUGH ( 12 FDA reports)
DYSGEUSIA ( 12 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 12 FDA reports)
FACE INJURY ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 12 FDA reports)
INCOHERENT ( 12 FDA reports)
INCREASED APPETITE ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
INTRA-UTERINE DEATH ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
MOTOR DYSFUNCTION ( 12 FDA reports)
PETIT MAL EPILEPSY ( 12 FDA reports)
RHINORRHOEA ( 12 FDA reports)
STENT OCCLUSION ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
ADVERSE EVENT ( 11 FDA reports)
ALCOHOL PROBLEM ( 11 FDA reports)
ANHEDONIA ( 11 FDA reports)
BLINDNESS ( 11 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 11 FDA reports)
FACIAL BONES FRACTURE ( 11 FDA reports)
FEELING HOT ( 11 FDA reports)
HEART RATE DECREASED ( 11 FDA reports)
HOSPITALISATION ( 11 FDA reports)
HYPOTHYROIDISM ( 11 FDA reports)
INHIBITORY DRUG INTERACTION ( 11 FDA reports)
MACROCYTOSIS ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 11 FDA reports)
MYOCARDITIS ( 11 FDA reports)
NASOPHARYNGITIS ( 11 FDA reports)
NIGHT SWEATS ( 11 FDA reports)
PIRIFORMIS SYNDROME ( 11 FDA reports)
POOR QUALITY SLEEP ( 11 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 11 FDA reports)
RETCHING ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 11 FDA reports)
THROAT TIGHTNESS ( 11 FDA reports)
ACCIDENT ( 10 FDA reports)
ADVERSE DRUG REACTION ( 10 FDA reports)
ARTERIOSCLEROSIS ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
COMPARTMENT SYNDROME ( 10 FDA reports)
DELIRIUM TREMENS ( 10 FDA reports)
DIALYSIS ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 10 FDA reports)
DRY SKIN ( 10 FDA reports)
DYSPHEMIA ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 10 FDA reports)
HIATUS HERNIA ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
HYPOVENTILATION ( 10 FDA reports)
IMMUNE SYSTEM DISORDER ( 10 FDA reports)
JOINT INJURY ( 10 FDA reports)
LOCALISED OEDEMA ( 10 FDA reports)
LOGORRHOEA ( 10 FDA reports)
MECHANICAL VENTILATION ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
NECK PAIN ( 10 FDA reports)
NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PANCREATIC DISORDER ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
PUPIL FIXED ( 10 FDA reports)
RESTLESS LEGS SYNDROME ( 10 FDA reports)
SPONDYLITIS ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
WRONG DRUG ADMINISTERED ( 10 FDA reports)
ABDOMINAL SYMPTOM ( 9 FDA reports)
ABDOMINAL WALL MASS ( 9 FDA reports)
ANKLE FRACTURE ( 9 FDA reports)
ANXIETY DISORDER ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 9 FDA reports)
BREAST MASS ( 9 FDA reports)
BREATH ODOUR ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONVERSION DISORDER ( 9 FDA reports)
CYTOLYTIC HEPATITIS ( 9 FDA reports)
DROWNING ( 9 FDA reports)
DYSKINESIA ( 9 FDA reports)
ERUCTATION ( 9 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 9 FDA reports)
EYE INFECTION ( 9 FDA reports)
GALLBLADDER POLYP ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
LACRIMATION INCREASED ( 9 FDA reports)
LESION EXCISION ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 9 FDA reports)
NEURALGIA ( 9 FDA reports)
OEDEMA ( 9 FDA reports)
OSTEONECROSIS OF JAW ( 9 FDA reports)
OTITIS MEDIA ( 9 FDA reports)
PANCREATIC CYST ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
THROMBOCYTHAEMIA ( 9 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
TRAUMATIC BRAIN INJURY ( 9 FDA reports)
URINARY RETENTION ( 9 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 8 FDA reports)
BLOOD LACTIC ACID INCREASED ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 8 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 8 FDA reports)
CARBON MONOXIDE POISONING ( 8 FDA reports)
CATARACT ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
COMA SCALE ABNORMAL ( 8 FDA reports)
DEAFNESS ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DRUG ADMINISTRATION ERROR ( 8 FDA reports)
DYSTONIA ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 8 FDA reports)
ELEVATED MOOD ( 8 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GENERALISED ANXIETY DISORDER ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
HEPATOCELLULAR INJURY ( 8 FDA reports)
HEPATOSPLENOMEGALY ( 8 FDA reports)
HYDROCELE ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
JOINT SWELLING ( 8 FDA reports)
LEFT ATRIAL DILATATION ( 8 FDA reports)
MASTOCYTOSIS ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
MURDER ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PANIC REACTION ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
POLYDACTYLY ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
SCAR ( 8 FDA reports)
SKULL FRACTURED BASE ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
VERBAL ABUSE ( 8 FDA reports)
VESTIBULAR DISORDER ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ALCOHOLIC LIVER DISEASE ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ATRIAL FLUTTER ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 7 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
BRAIN HYPOXIA ( 7 FDA reports)
CARBON DIOXIDE DECREASED ( 7 FDA reports)
CIRRHOSIS ALCOHOLIC ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DERMATITIS CONTACT ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
ENERGY INCREASED ( 7 FDA reports)
EYE DISORDER ( 7 FDA reports)
FLASHBACK ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 7 FDA reports)
HYPOTONIA ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
OCCULT BLOOD POSITIVE ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
POLYSUBSTANCE ABUSE ( 7 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 7 FDA reports)
POSTURE ABNORMAL ( 7 FDA reports)
POSTURING ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RETROGRADE AMNESIA ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 7 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 7 FDA reports)
SLEEP-RELATED EATING DISORDER ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
SURGERY ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ADVERSE REACTION ( 6 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BLOOD ETHANOL INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PH INCREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
BRUXISM ( 6 FDA reports)
CARDIAC FLUTTER ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CEREBRAL ISCHAEMIA ( 6 FDA reports)
CHILD ABUSE ( 6 FDA reports)
CHLAMYDIAL INFECTION ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
DYSMORPHISM ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYE PENETRATION ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FISTULA ( 6 FDA reports)
FLIGHT OF IDEAS ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
GLARE ( 6 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 6 FDA reports)
GRIEF REACTION ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPERMETROPIA ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
INGROWING NAIL ( 6 FDA reports)
INJURY ASPHYXIATION ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
JUDGEMENT IMPAIRED ( 6 FDA reports)
LEARNING DISORDER ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
MULTIPLE INJURIES ( 6 FDA reports)
NARCOTIC INTOXICATION ( 6 FDA reports)
NEGATIVE THOUGHTS ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
PNEUMOCEPHALUS ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
POST PROCEDURAL PNEUMONIA ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
SMOKER ( 6 FDA reports)
SNORING ( 6 FDA reports)
SOFT TISSUE INJURY ( 6 FDA reports)
SPINAL X-RAY ABNORMAL ( 6 FDA reports)
SPUTUM ABNORMAL ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
TENSION ( 6 FDA reports)
THERMAL BURN ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VICTIM OF HOMICIDE ( 6 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABORTION INDUCED ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ALCOHOLIC ( 5 FDA reports)
ALCOHOLIC PANCREATITIS ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANTICHOLINERGIC SYNDROME ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 5 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BOWEL SOUNDS ABNORMAL ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COLON POLYPECTOMY ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DEVICE LEAKAGE ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DIZZINESS POSTURAL ( 5 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
FOETAL GROWTH RESTRICTION ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
FRUSTRATION ( 5 FDA reports)
GASTRIC LAVAGE ( 5 FDA reports)
GRANDIOSITY ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAIR METAL TEST ABNORMAL ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATITIS ALCOHOLIC ( 5 FDA reports)
HIP DYSPLASIA ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INTRAOCULAR LENS IMPLANT ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
LEG AMPUTATION ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LOSS OF EMPLOYMENT ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MOANING ( 5 FDA reports)
MORBID THOUGHTS ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 5 FDA reports)
MYOPATHY ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
ORAL SURGERY ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PARASOMNIA ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
SPINA BIFIDA ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STUPOR ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
VERTEBROPLASTY ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
VITREOUS FLOATERS ( 5 FDA reports)
ACNE ( 4 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
ALCOHOLIC SEIZURE ( 4 FDA reports)
ANAESTHESIA REVERSAL ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTEROGRADE AMNESIA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BLINDNESS TRANSIENT ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD ALCOHOL ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 4 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CATHETER PLACEMENT ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CEREBRAL PALSY ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CHOLESTATIC PRURITUS ( 4 FDA reports)
CONGENITAL HEPATOMEGALY ( 4 FDA reports)
CONGENITAL TERATOMA ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
ERECTION INCREASED ( 4 FDA reports)
EROSIVE OESOPHAGITIS ( 4 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEELING GUILTY ( 4 FDA reports)
FOETAL ALCOHOL SYNDROME ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INDUCED LABOUR ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
MENINGOMYELOCELE ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MICTURITION DISORDER ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PYROMANIA ( 4 FDA reports)
RECTAL PROLAPSE ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
STAB WOUND ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TERATOMA ( 4 FDA reports)
THIRST ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ACETABULUM FRACTURE ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
APHONIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLOOD ALCOHOL ABNORMAL ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIOTOXICITY ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHORIOAMNIONITIS ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
COMPULSIONS ( 3 FDA reports)
CONGENITAL NYSTAGMUS ( 3 FDA reports)
CONGENITAL VISUAL ACUITY REDUCED ( 3 FDA reports)
COPROLALIA ( 3 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG LABEL CONFUSION ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
EAR MALFORMATION ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENERAL NUTRITION DISORDER ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GLUCOSE URINE ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATITIS C POSITIVE ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INTERNAL INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LIP INJURY ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MENDELSON'S SYNDROME ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
NODULE ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OLFACTORY NERVE DISORDER ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PANCREATITIS VIRAL ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PSEUDO-BARTTER SYNDROME ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SEXUAL ASSAULT VICTIM ( 3 FDA reports)
SEXUAL OFFENCE ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SPOUSAL ABUSE ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUDDEN VISUAL LOSS ( 3 FDA reports)
SWEAT DISCOLOURATION ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TRANCE ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
ULCER ( 3 FDA reports)
UMBILICAL CORD AROUND NECK ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VICTIM OF CRIME ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACCIDENTAL POISONING ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AGITATION NEONATAL ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AURA ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONGENITAL MEGAURETER ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGENITAL OCULOMOTOR APRAXIA ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CSF PROTEIN ( 2 FDA reports)
DELUSION OF REFERENCE ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIASTOLIC HYPOTENSION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG HALF-LIFE INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EPENDYMOMA ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXHIBITIONISM ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FACE CRUSHING ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FATTY LIVER ALCOHOLIC ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FILARIASIS ( 2 FDA reports)
FINGER HYPOPLASIA ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GASTRITIS ALCOHOLIC ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
IDIOSYNCRATIC ALCOHOL INTOXICATION ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MECONIUM PERITONITIS ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE GRAFT ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEONATAL RESPIRATORY ARREST ( 2 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC INFECTION ( 2 FDA reports)
PENILE PROSTHESIS INSERTION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL DYSPLASIA ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
SCAR EXCISION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SERUM SEROTONIN INCREASED ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN DYSTROPHY ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SLEEP SEX ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SYMPATHOMIMETIC EFFECT ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TIC ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VISION ABNORMAL NEONATAL ( 2 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOLISATION PROCEDURE ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA-2 MACROGLOBULIN INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC CAVITY DISORDER ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIRUBIN CONJUGATED ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BRONCHIAL INJURY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ATAXIA ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLINODACTYLY ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NAIL DISORDER ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONGENITAL URETHRAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORNEAL BLEB ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRIME ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAGLE BARRETT SYNDROME ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACTOR VII DEFICIENCY ( 1 FDA reports)
FACTOR X DEFICIENCY ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FONTANELLE DEPRESSED ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE VIII ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KNEE MENISCECTOMY ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LESION OF ULNAR NERVE ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOPROTEIN DEFICIENCY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL ALCOHOL USE ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MENARCHE ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEUROCYSTICERCOSIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION EXPOSURE DURING PREGNANCY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEXUAL INHIBITION ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN MALFORMATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN MALFORMATION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRAUMATIC DELIVERY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URETHRAL VALVES ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
X-LINKED CHROMOSOMAL DISORDER ( 1 FDA reports)

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