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

HEADACHE ( 64 FDA reports)
NAUSEA ( 62 FDA reports)
DYSPNOEA ( 44 FDA reports)
DRUG INEFFECTIVE ( 43 FDA reports)
FATIGUE ( 43 FDA reports)
RENAL FAILURE ACUTE ( 43 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 41 FDA reports)
CONVULSION ( 39 FDA reports)
VOMITING ( 39 FDA reports)
CONDITION AGGRAVATED ( 36 FDA reports)
HYPOTENSION ( 35 FDA reports)
ANAEMIA ( 34 FDA reports)
CONFUSIONAL STATE ( 33 FDA reports)
DIARRHOEA ( 33 FDA reports)
VISUAL ACUITY REDUCED ( 33 FDA reports)
ASTHENIA ( 32 FDA reports)
ATRIAL FIBRILLATION ( 32 FDA reports)
DIZZINESS ( 31 FDA reports)
RENAL FAILURE ( 28 FDA reports)
SPEECH DISORDER ( 28 FDA reports)
SOMNOLENCE ( 27 FDA reports)
PAIN ( 26 FDA reports)
PNEUMONIA ( 26 FDA reports)
GRAND MAL CONVULSION ( 25 FDA reports)
DEPRESSION ( 24 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 24 FDA reports)
FEAR ( 24 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 23 FDA reports)
DEHYDRATION ( 23 FDA reports)
FEELING ABNORMAL ( 23 FDA reports)
FALL ( 22 FDA reports)
SUICIDAL IDEATION ( 22 FDA reports)
NERVOUSNESS ( 21 FDA reports)
VISION BLURRED ( 21 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
METABOLIC ACIDOSIS ( 20 FDA reports)
GLAUCOMA ( 19 FDA reports)
CARDIAC ANEURYSM ( 18 FDA reports)
LIVER DISORDER ( 18 FDA reports)
HYPERTENSION ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
ACUTE RESPIRATORY FAILURE ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 16 FDA reports)
RASH ( 16 FDA reports)
CARDIAC TAMPONADE ( 15 FDA reports)
CATARACT ( 15 FDA reports)
CHEST PAIN ( 15 FDA reports)
DEATH ( 15 FDA reports)
DEEP VEIN THROMBOSIS ( 15 FDA reports)
MUSCLE TWITCHING ( 15 FDA reports)
PYREXIA ( 15 FDA reports)
WEIGHT DECREASED ( 15 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
CHOLELITHIASIS ( 14 FDA reports)
PARAESTHESIA ( 14 FDA reports)
PERICARDIAL HAEMORRHAGE ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
ACIDOSIS ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ARRHYTHMIA ( 13 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
CARDIO-RESPIRATORY ARREST ( 13 FDA reports)
EMOTIONAL DISTRESS ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
INTRA-UTERINE DEATH ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
RETINAL HAEMORRHAGE ( 13 FDA reports)
CARDIOGENIC SHOCK ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
OSTEOPENIA ( 12 FDA reports)
PULMONARY HYPERTENSION ( 12 FDA reports)
TREMOR ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASTHMA ( 11 FDA reports)
BACK PAIN ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CALCIUM DEFICIENCY ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
ENDOTRACHEAL INTUBATION ( 11 FDA reports)
GALLBLADDER DISORDER ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
OSTEOPOROSIS ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
SKIN CANCER ( 11 FDA reports)
VITAMIN D DEFICIENCY ( 11 FDA reports)
AZOTAEMIA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BLINDNESS ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
ECONOMIC PROBLEM ( 10 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 10 FDA reports)
EYE PAIN ( 10 FDA reports)
GAIT DISTURBANCE ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
HYSTERECTOMY ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
POSTPARTUM HAEMORRHAGE ( 10 FDA reports)
RETINOPATHY ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
AGITATION ( 9 FDA reports)
ANXIETY ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CARDIAC OUTPUT DECREASED ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
CORNEAL OEDEMA ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
GANGRENE ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
INCORRECT DOSE ADMINISTERED ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
ABORTION SPONTANEOUS ( 8 FDA reports)
ATRIAL FLUTTER ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CONJUNCTIVITIS ( 8 FDA reports)
COUGH ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
EYE OEDEMA ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
INJURY ( 8 FDA reports)
IRIDOCYCLITIS ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
MULTIPLE INJURIES ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CHOROIDAL DETACHMENT ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
ELECTROLYTE IMBALANCE ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
EYE DISORDER ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
MACROCYTOSIS ( 7 FDA reports)
MIOSIS ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
ANTERIOR CHAMBER DISORDER ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CARDIORENAL SYNDROME ( 6 FDA reports)
CATARACT OPERATION ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
COMA ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPHAEMA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SWELLING ( 6 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 6 FDA reports)
UVEITIS ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
ABNORMAL DREAMS ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CHOROIDAL EFFUSION ( 5 FDA reports)
CORNEAL OPACITY ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
DEPRESSION SUICIDAL ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FOETAL DISORDER ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
GOUT ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
POLYURIA ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
SERRATIA SEPSIS ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SOMATIC HALLUCINATION ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONJUNCTIVAL OEDEMA ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORNEAL GRAFT REJECTION ( 4 FDA reports)
CYST ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIABETIC NEPHROPATHY ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CLEFT LIP AND PALATE ( 3 FDA reports)
CLEFT PALATE ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GONORRHOEA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LINEAR IGA DISEASE ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METASTASES TO PLEURA ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OCULAR VASCULITIS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PAROPHTHALMIA ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
ROTAVIRUS INFECTION ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOROIDAL HAEMORRHAGE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORNEAL TOUCH ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 2 FDA reports)
LENS DISORDER ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOCOAGULATION ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRABECULECTOMY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BROMODERMA ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL DECREASED ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHORIOCARCINOMA ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL INTESTINAL MALFORMATION ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORECTOPIA ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL EXFOLIATION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE BALANITIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEEDING PROBLEM IN CHILD ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTONY OF EYE ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IRIDECTOMY ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS NEOVASCULARISATION ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS I ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OPHTHALMIC FLUID DRAINAGE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UVEAL EFFUSION SYNDROME ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VULVAL HAEMATOMA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
YAWNING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use