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

PYREXIA ( 91 FDA reports)
TREMOR ( 78 FDA reports)
HALLUCINATION ( 69 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 68 FDA reports)
FALL ( 67 FDA reports)
SOMNOLENCE ( 65 FDA reports)
WEIGHT INCREASED ( 65 FDA reports)
DYSKINESIA ( 61 FDA reports)
DIABETES MELLITUS ( 59 FDA reports)
ABNORMAL BEHAVIOUR ( 56 FDA reports)
CONDITION AGGRAVATED ( 55 FDA reports)
DEPRESSION ( 55 FDA reports)
NAUSEA ( 50 FDA reports)
RHABDOMYOLYSIS ( 50 FDA reports)
DYSPNOEA ( 49 FDA reports)
FATIGUE ( 48 FDA reports)
DRUG INEFFECTIVE ( 47 FDA reports)
PNEUMONIA ( 46 FDA reports)
AGGRESSION ( 44 FDA reports)
ASTHENIA ( 42 FDA reports)
DIZZINESS ( 42 FDA reports)
MALAISE ( 42 FDA reports)
HEADACHE ( 41 FDA reports)
VOMITING ( 40 FDA reports)
ANXIETY ( 39 FDA reports)
DELUSION ( 39 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 38 FDA reports)
CONVULSION ( 38 FDA reports)
AGITATION ( 37 FDA reports)
CONSTIPATION ( 37 FDA reports)
DEHYDRATION ( 37 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 37 FDA reports)
INSOMNIA ( 36 FDA reports)
TARDIVE DYSKINESIA ( 36 FDA reports)
DIARRHOEA ( 35 FDA reports)
DYSPHAGIA ( 35 FDA reports)
GAIT DISTURBANCE ( 35 FDA reports)
HALLUCINATION, AUDITORY ( 35 FDA reports)
HYPONATRAEMIA ( 34 FDA reports)
DRUG INTERACTION ( 33 FDA reports)
TACHYCARDIA ( 33 FDA reports)
PAIN ( 32 FDA reports)
SPEECH DISORDER ( 32 FDA reports)
FEELING ABNORMAL ( 31 FDA reports)
PATHOLOGICAL GAMBLING ( 30 FDA reports)
LOSS OF CONSCIOUSNESS ( 29 FDA reports)
WEIGHT DECREASED ( 29 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 28 FDA reports)
CONFUSIONAL STATE ( 28 FDA reports)
HYPERTENSION ( 28 FDA reports)
PARKINSON'S DISEASE ( 28 FDA reports)
PLEURAL EFFUSION ( 28 FDA reports)
RENAL FAILURE ACUTE ( 28 FDA reports)
SUDDEN ONSET OF SLEEP ( 28 FDA reports)
TYPE 2 DIABETES MELLITUS ( 28 FDA reports)
OVERDOSE ( 27 FDA reports)
PNEUMONIA ASPIRATION ( 27 FDA reports)
SUICIDAL IDEATION ( 27 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 26 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 26 FDA reports)
MUSCULAR WEAKNESS ( 25 FDA reports)
TREATMENT NONCOMPLIANCE ( 25 FDA reports)
OEDEMA PERIPHERAL ( 24 FDA reports)
PALPITATIONS ( 24 FDA reports)
PSYCHOTIC DISORDER ( 24 FDA reports)
BLOOD GLUCOSE INCREASED ( 23 FDA reports)
DELIRIUM ( 23 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 23 FDA reports)
MITRAL VALVE INCOMPETENCE ( 23 FDA reports)
ROAD TRAFFIC ACCIDENT ( 23 FDA reports)
AMNESIA ( 22 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 22 FDA reports)
PANCREATITIS ( 22 FDA reports)
RESTLESSNESS ( 22 FDA reports)
BLOOD PRESSURE DECREASED ( 21 FDA reports)
DIABETIC KETOACIDOSIS ( 21 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 20 FDA reports)
HYPERGLYCAEMIA ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
PARAESTHESIA ( 20 FDA reports)
PSYCHIATRIC SYMPTOM ( 20 FDA reports)
VISION BLURRED ( 20 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 19 FDA reports)
EMOTIONAL DISTRESS ( 19 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
HAEMOGLOBIN DECREASED ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
MENTAL DISORDER ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
BACK PAIN ( 18 FDA reports)
DEATH ( 18 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
HAEMATOCRIT DECREASED ( 18 FDA reports)
HYPOGLYCAEMIA ( 18 FDA reports)
MEMORY IMPAIRMENT ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
AORTIC VALVE INCOMPETENCE ( 17 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
COUGH ( 17 FDA reports)
GASTROINTESTINAL DISORDER ( 17 FDA reports)
HYPOAESTHESIA ( 17 FDA reports)
HYPOXIA ( 17 FDA reports)
INTESTINAL OBSTRUCTION ( 17 FDA reports)
MUSCLE RIGIDITY ( 17 FDA reports)
RASH ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 16 FDA reports)
CARDIO-RESPIRATORY ARREST ( 16 FDA reports)
CHEST PAIN ( 16 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 16 FDA reports)
ECONOMIC PROBLEM ( 16 FDA reports)
EMOTIONAL DISORDER ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
THROMBOCYTOPENIA ( 16 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 16 FDA reports)
ANGER ( 15 FDA reports)
HYPERTHERMIA ( 15 FDA reports)
HYPOTONIA ( 15 FDA reports)
INTERSTITIAL LUNG DISEASE ( 15 FDA reports)
LEUKOPENIA ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
PRURITUS ( 15 FDA reports)
SYNCOPE ( 15 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 15 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
COMPLETED SUICIDE ( 14 FDA reports)
OBESITY ( 14 FDA reports)
BLOOD SODIUM DECREASED ( 13 FDA reports)
CONTUSION ( 13 FDA reports)
DISORIENTATION ( 13 FDA reports)
DYSTONIA ( 13 FDA reports)
HALLUCINATION, VISUAL ( 13 FDA reports)
MOVEMENT DISORDER ( 13 FDA reports)
PANIC ATTACK ( 13 FDA reports)
POLLAKIURIA ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
ABASIA ( 12 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
CARDIOMYOPATHY ( 12 FDA reports)
CYTOLYTIC HEPATITIS ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
DIABETIC NEUROPATHY ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
HYPERPHAGIA ( 12 FDA reports)
LUNG DISORDER ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
NERVOUS SYSTEM DISORDER ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PULMONARY OEDEMA ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
URINARY INCONTINENCE ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
DRUG EFFECT DECREASED ( 11 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MUSCLE DISORDER ( 11 FDA reports)
MUSCLE TWITCHING ( 11 FDA reports)
MUTISM ( 11 FDA reports)
NERVOUSNESS ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SHOCK ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
AFFECT LABILITY ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
COMPULSIONS ( 10 FDA reports)
DEMENTIA ( 10 FDA reports)
DISTURBANCE IN ATTENTION ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
EYELID PTOSIS ( 10 FDA reports)
FEAR ( 10 FDA reports)
FLATULENCE ( 10 FDA reports)
HYPERSEXUALITY ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
MENTAL IMPAIRMENT ( 10 FDA reports)
MYOCLONUS ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
ORTHOSTATIC HYPOTENSION ( 10 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 10 FDA reports)
SCHIZOPHRENIA ( 10 FDA reports)
SEDATION ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
AKINESIA ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CARDIAC VALVE DISEASE ( 9 FDA reports)
CEREBRAL ATROPHY ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DIABETIC RETINOPATHY ( 9 FDA reports)
DRY MOUTH ( 9 FDA reports)
DYSSTASIA ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
GAMBLING ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
ILEUS ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
MUSCLE TIGHTNESS ( 9 FDA reports)
NEUTROPHIL COUNT DECREASED ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
AGRANULOCYTOSIS ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CHOKING ( 8 FDA reports)
COLON INJURY ( 8 FDA reports)
DEPRESSED MOOD ( 8 FDA reports)
DIABETIC GASTROPARESIS ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
GASTROINTESTINAL INJURY ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
GRANULOCYTOPENIA ( 8 FDA reports)
HEPATITIS FULMINANT ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INCOHERENT ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
PANIC DISORDER ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
PERSECUTORY DELUSION ( 8 FDA reports)
PERSONALITY CHANGE ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
THIRST ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
AKATHISIA ( 7 FDA reports)
APALLIC SYNDROME ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
COMA ( 7 FDA reports)
CRYING ( 7 FDA reports)
DRUG ABUSER ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INFLAMMATION ( 7 FDA reports)
INJURY ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
PARKINSONIAN GAIT ( 7 FDA reports)
PO2 DECREASED ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
STUPOR ( 7 FDA reports)
TALIPES ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
TORTICOLLIS ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
BINGE EATING ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD OESTROGEN DECREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
HORMONE LEVEL ABNORMAL ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOTONIA NEONATAL ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PREMENSTRUAL SYNDROME ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
ADRENAL DISORDER ( 5 FDA reports)
AMENORRHOEA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHOREA ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
IMPLANT SITE EFFUSION ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MANIA ( 5 FDA reports)
MASKED FACIES ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RETCHING ( 5 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ACNE ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHROMATOPSIA ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG LEVEL DECREASED ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
GENITOURINARY TRACT INFECTION ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENOMETRORRHAGIA ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SOMNOLENCE NEONATAL ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
STRESS ( 4 FDA reports)
SUPRANUCLEAR PALSY ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
WATER INTOXICATION ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
APATHY ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIRUBINURIA ( 3 FDA reports)
BIOPSY SKIN ( 3 FDA reports)
BLADDER DILATATION ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEMENTIA WITH LEWY BODIES ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DISSOCIATIVE FUGUE ( 3 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NIEMANN-PICK DISEASE ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PHARYNGEAL ABSCESS ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
RALES ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SCROTAL HAEMATOCOELE ( 3 FDA reports)
SELF MUTILATION ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SWELLING ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALPHA GLOBULIN INCREASED ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLUTTERING ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEEP BRAIN STIMULATION ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EUSTACHIAN TUBE DISORDER ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FEVER NEONATAL ( 2 FDA reports)
FORCEPS DELIVERY ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFUSION SITE BRUISING ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 2 FDA reports)
MEGACOLON ACQUIRED ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MOANING ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEXUAL ACTIVITY INCREASED ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO DECREASED ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANO-RECTAL STENOSIS ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AUTISM ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BANKRUPTCY ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR VII DEFICIENCY ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA TEETH ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE DECREASED ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NYMPHOMANIA ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PICA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEDATIVE THERAPY ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL CANCER STAGE III ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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