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

ANXIETY ( 29 FDA reports)
DEPRESSION ( 25 FDA reports)
SUICIDAL IDEATION ( 25 FDA reports)
COGNITIVE DISORDER ( 24 FDA reports)
DRUG INTERACTION ( 24 FDA reports)
AGITATION ( 21 FDA reports)
ASTHENIA ( 21 FDA reports)
HYPOTENSION ( 20 FDA reports)
AMNESIA ( 19 FDA reports)
DISTURBANCE IN ATTENTION ( 19 FDA reports)
FATIGUE ( 19 FDA reports)
HEADACHE ( 19 FDA reports)
INSOMNIA ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
VOMITING ( 17 FDA reports)
AGGRESSION ( 16 FDA reports)
DIZZINESS ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
MALAISE ( 16 FDA reports)
MEMORY IMPAIRMENT ( 16 FDA reports)
SPEECH DISORDER ( 16 FDA reports)
OVERDOSE ( 15 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
CONSTIPATION ( 14 FDA reports)
FALL ( 14 FDA reports)
NIGHTMARE ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ILEUS PARALYTIC ( 12 FDA reports)
IRRITABILITY ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
ANGER ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
RASH ( 11 FDA reports)
TREMOR ( 11 FDA reports)
ANOREXIA ( 10 FDA reports)
APATHY ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
COAGULOPATHY ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
DRUG ABUSER ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
FEAR ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
GRAND MAL CONVULSION ( 9 FDA reports)
PAIN ( 9 FDA reports)
TREATMENT NONCOMPLIANCE ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
DELUSION ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
DRUG DEPENDENCE ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ALCOHOLISM ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
FLUID INTAKE REDUCED ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ANAEMIA ( 6 FDA reports)
BLOOD ALCOHOL INCREASED ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
COMA ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
MANIA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INJURY ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
POLYSUBSTANCE ABUSE ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SELF MUTILATION ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ACNE ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ALCOHOL INTOLERANCE ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BRADYPHRENIA ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MELAENA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SELF-INJURIOUS IDEATION ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CRYING ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPERGER'S DISORDER ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POISONING ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BED REST ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACTOR X DEFICIENCY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
URINE BARBITURATES ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)

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