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

VOMITING ( 276 FDA reports)
NAUSEA ( 243 FDA reports)
HYPOTENSION ( 211 FDA reports)
PAIN ( 196 FDA reports)
CARDIAC ARREST ( 189 FDA reports)
BRADYCARDIA ( 182 FDA reports)
DYSPNOEA ( 175 FDA reports)
ANXIETY ( 163 FDA reports)
RENAL FAILURE ( 159 FDA reports)
PYREXIA ( 154 FDA reports)
DIARRHOEA ( 149 FDA reports)
HYPERTHERMIA ( 136 FDA reports)
PNEUMONIA ( 132 FDA reports)
INJURY ( 131 FDA reports)
ASTHENIA ( 118 FDA reports)
RENAL FAILURE ACUTE ( 117 FDA reports)
ANAEMIA ( 115 FDA reports)
DEATH ( 115 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 111 FDA reports)
DIZZINESS ( 110 FDA reports)
RESPIRATORY FAILURE ( 110 FDA reports)
THROMBOCYTOPENIA ( 106 FDA reports)
DEHYDRATION ( 105 FDA reports)
FATIGUE ( 105 FDA reports)
MYOCARDIAL INFARCTION ( 101 FDA reports)
CONFUSIONAL STATE ( 100 FDA reports)
ATRIAL FIBRILLATION ( 98 FDA reports)
FALL ( 96 FDA reports)
SEPSIS ( 91 FDA reports)
VENTRICULAR FIBRILLATION ( 91 FDA reports)
HYPERTENSION ( 90 FDA reports)
DEEP VEIN THROMBOSIS ( 89 FDA reports)
ABDOMINAL PAIN ( 85 FDA reports)
HEADACHE ( 84 FDA reports)
OEDEMA PERIPHERAL ( 84 FDA reports)
CARDIO-RESPIRATORY ARREST ( 81 FDA reports)
LOSS OF CONSCIOUSNESS ( 79 FDA reports)
PLEURAL EFFUSION ( 79 FDA reports)
VENTRICULAR TACHYCARDIA ( 79 FDA reports)
TACHYCARDIA ( 78 FDA reports)
UNEVALUABLE EVENT ( 78 FDA reports)
MULTI-ORGAN FAILURE ( 77 FDA reports)
DEPRESSION ( 76 FDA reports)
CHEST PAIN ( 74 FDA reports)
DRUG INEFFECTIVE ( 72 FDA reports)
CEREBROVASCULAR ACCIDENT ( 71 FDA reports)
ECONOMIC PROBLEM ( 71 FDA reports)
CONVULSION ( 70 FDA reports)
WEIGHT DECREASED ( 69 FDA reports)
ARRHYTHMIA ( 68 FDA reports)
MALAISE ( 68 FDA reports)
PULMONARY EMBOLISM ( 67 FDA reports)
BACK PAIN ( 66 FDA reports)
ANHEDONIA ( 65 FDA reports)
DRUG INTERACTION ( 64 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 64 FDA reports)
CORONARY ARTERY DISEASE ( 63 FDA reports)
PULMONARY OEDEMA ( 62 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 61 FDA reports)
ARTHRALGIA ( 60 FDA reports)
DECREASED APPETITE ( 59 FDA reports)
DRUG TOXICITY ( 59 FDA reports)
DYSPHAGIA ( 59 FDA reports)
EMOTIONAL DISTRESS ( 58 FDA reports)
FEAR ( 58 FDA reports)
HYPOXIA ( 58 FDA reports)
OXYGEN SATURATION DECREASED ( 57 FDA reports)
INSOMNIA ( 56 FDA reports)
URINARY TRACT INFECTION ( 56 FDA reports)
BLOOD PRESSURE DECREASED ( 55 FDA reports)
RASH ( 55 FDA reports)
SOMNOLENCE ( 55 FDA reports)
ATELECTASIS ( 53 FDA reports)
GAIT DISTURBANCE ( 53 FDA reports)
CARDIOGENIC SHOCK ( 52 FDA reports)
UNRESPONSIVE TO STIMULI ( 52 FDA reports)
CARDIOMEGALY ( 51 FDA reports)
CONSTIPATION ( 51 FDA reports)
MULTIPLE INJURIES ( 51 FDA reports)
AGITATION ( 50 FDA reports)
CHILLS ( 50 FDA reports)
COUGH ( 50 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 50 FDA reports)
PAIN IN EXTREMITY ( 49 FDA reports)
MUSCULAR WEAKNESS ( 48 FDA reports)
DISORIENTATION ( 47 FDA reports)
RENAL IMPAIRMENT ( 47 FDA reports)
RESPIRATORY ARREST ( 47 FDA reports)
CONDITION AGGRAVATED ( 46 FDA reports)
HYPOAESTHESIA ( 46 FDA reports)
MENTAL STATUS CHANGES ( 46 FDA reports)
MITRAL VALVE INCOMPETENCE ( 45 FDA reports)
HAEMOGLOBIN DECREASED ( 44 FDA reports)
NEUTROPENIA ( 44 FDA reports)
POST PROCEDURAL COMPLICATION ( 44 FDA reports)
SINUS TACHYCARDIA ( 44 FDA reports)
ABDOMINAL DISTENSION ( 43 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 43 FDA reports)
CARDIAC FAILURE ( 43 FDA reports)
HEART RATE INCREASED ( 43 FDA reports)
BONE DISORDER ( 42 FDA reports)
ERYTHEMA ( 42 FDA reports)
PULMONARY HYPERTENSION ( 42 FDA reports)
SYNCOPE ( 42 FDA reports)
HYPERHIDROSIS ( 41 FDA reports)
CYANOSIS ( 40 FDA reports)
DYSARTHRIA ( 40 FDA reports)
HYPERKALAEMIA ( 40 FDA reports)
URINARY INCONTINENCE ( 40 FDA reports)
CELLULITIS ( 39 FDA reports)
OSTEONECROSIS OF JAW ( 39 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 39 FDA reports)
HYPERSENSITIVITY ( 38 FDA reports)
RENAL FAILURE CHRONIC ( 38 FDA reports)
STRESS ( 38 FDA reports)
BALANCE DISORDER ( 37 FDA reports)
BLOOD PRESSURE INCREASED ( 37 FDA reports)
CEREBRAL INFARCTION ( 37 FDA reports)
HYPOPHAGIA ( 37 FDA reports)
LOOSE TOOTH ( 37 FDA reports)
MYOCARDIAL ISCHAEMIA ( 37 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 37 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 36 FDA reports)
BLOOD GLUCOSE INCREASED ( 36 FDA reports)
BLOOD POTASSIUM DECREASED ( 36 FDA reports)
BRONCHITIS ( 36 FDA reports)
METASTASES TO BONE ( 36 FDA reports)
PARAESTHESIA ( 36 FDA reports)
SEDATION ( 36 FDA reports)
APNOEA ( 35 FDA reports)
FEBRILE NEUTROPENIA ( 35 FDA reports)
HYPONATRAEMIA ( 35 FDA reports)
SEPTIC SHOCK ( 35 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 34 FDA reports)
GASTRITIS ( 34 FDA reports)
HAEMORRHAGE ( 34 FDA reports)
METABOLIC ACIDOSIS ( 34 FDA reports)
RENAL INJURY ( 34 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 33 FDA reports)
HEART RATE IRREGULAR ( 33 FDA reports)
VISION BLURRED ( 33 FDA reports)
WEIGHT INCREASED ( 33 FDA reports)
BLOOD CREATININE INCREASED ( 32 FDA reports)
CARDIOMYOPATHY ( 32 FDA reports)
COMA ( 32 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 32 FDA reports)
PALPITATIONS ( 32 FDA reports)
RHABDOMYOLYSIS ( 32 FDA reports)
CEREBRAL HAEMORRHAGE ( 31 FDA reports)
HYPOKALAEMIA ( 31 FDA reports)
NEUROPATHY PERIPHERAL ( 31 FDA reports)
OVERDOSE ( 31 FDA reports)
PANCYTOPENIA ( 31 FDA reports)
SINUS BRADYCARDIA ( 31 FDA reports)
CARDIAC DISORDER ( 30 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 30 FDA reports)
MYDRIASIS ( 30 FDA reports)
PAIN IN JAW ( 30 FDA reports)
PRURITUS ( 30 FDA reports)
SWELLING ( 30 FDA reports)
THROMBOSIS ( 30 FDA reports)
TREMOR ( 30 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 29 FDA reports)
CIRCULATORY COLLAPSE ( 29 FDA reports)
COAGULOPATHY ( 29 FDA reports)
LETHARGY ( 29 FDA reports)
ANAPHYLACTIC REACTION ( 28 FDA reports)
ANAPHYLACTIC SHOCK ( 28 FDA reports)
DYSPEPSIA ( 28 FDA reports)
ENCEPHALOPATHY ( 28 FDA reports)
MUSCULOSKELETAL PAIN ( 28 FDA reports)
NECK PAIN ( 28 FDA reports)
OEDEMA ( 28 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 28 FDA reports)
BLOOD CALCIUM DECREASED ( 27 FDA reports)
DIABETES MELLITUS ( 27 FDA reports)
HEPATIC FAILURE ( 27 FDA reports)
SPINAL OSTEOARTHRITIS ( 27 FDA reports)
ABDOMINAL PAIN UPPER ( 26 FDA reports)
AMNESIA ( 26 FDA reports)
ANGINA PECTORIS ( 26 FDA reports)
ARTERIOSCLEROSIS ( 26 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 26 FDA reports)
ENDOTRACHEAL INTUBATION ( 26 FDA reports)
HAEMATOMA ( 26 FDA reports)
HYPERGLYCAEMIA ( 26 FDA reports)
IMPAIRED HEALING ( 26 FDA reports)
JAW DISORDER ( 26 FDA reports)
MOBILITY DECREASED ( 26 FDA reports)
PLATELET COUNT DECREASED ( 26 FDA reports)
RESPIRATORY DEPRESSION ( 26 FDA reports)
TORSADE DE POINTES ( 26 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 26 FDA reports)
VISUAL IMPAIRMENT ( 26 FDA reports)
ACUTE RESPIRATORY FAILURE ( 25 FDA reports)
CONTUSION ( 25 FDA reports)
FAECAL INCONTINENCE ( 25 FDA reports)
INFECTION ( 25 FDA reports)
RESPIRATORY DISORDER ( 25 FDA reports)
RESPIRATORY DISTRESS ( 25 FDA reports)
SHOCK ( 25 FDA reports)
TOOTH LOSS ( 25 FDA reports)
ASTHMA ( 24 FDA reports)
BLOOD ALBUMIN DECREASED ( 24 FDA reports)
LEUKOCYTOSIS ( 24 FDA reports)
SKIN DISORDER ( 24 FDA reports)
BONE LESION ( 23 FDA reports)
COMPRESSION FRACTURE ( 23 FDA reports)
HEART RATE DECREASED ( 23 FDA reports)
HYPOTHYROIDISM ( 23 FDA reports)
MALNUTRITION ( 23 FDA reports)
PERICARDIAL EFFUSION ( 23 FDA reports)
PROCEDURAL COMPLICATION ( 23 FDA reports)
ACUTE CORONARY SYNDROME ( 22 FDA reports)
ARTHRITIS ( 22 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 22 FDA reports)
DYSKINESIA ( 22 FDA reports)
FLUSHING ( 22 FDA reports)
HAEMATURIA ( 22 FDA reports)
RECTAL HAEMORRHAGE ( 22 FDA reports)
TOOTH EXTRACTION ( 22 FDA reports)
CARPAL TUNNEL SYNDROME ( 21 FDA reports)
DEMENTIA ( 21 FDA reports)
DISEASE PROGRESSION ( 21 FDA reports)
DRUG HYPERSENSITIVITY ( 21 FDA reports)
HIP FRACTURE ( 21 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 21 FDA reports)
JAW FRACTURE ( 21 FDA reports)
LIVER DISORDER ( 21 FDA reports)
OSTEOMYELITIS ( 21 FDA reports)
PULMONARY CONGESTION ( 21 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
ANAESTHETIC COMPLICATION ( 20 FDA reports)
ASCITES ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 20 FDA reports)
BONE PAIN ( 20 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 20 FDA reports)
CUBITAL TUNNEL SYNDROME ( 20 FDA reports)
DISCOMFORT ( 20 FDA reports)
INFUSION RELATED REACTION ( 20 FDA reports)
JUGULAR VEIN THROMBOSIS ( 20 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 20 FDA reports)
MENTAL DISORDER ( 20 FDA reports)
ODYNOPHAGIA ( 20 FDA reports)
ORAL PAIN ( 20 FDA reports)
RENAL TUBULAR NECROSIS ( 20 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 20 FDA reports)
AGGRESSION ( 19 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 19 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
BRONCHOSPASM ( 19 FDA reports)
CHEST DISCOMFORT ( 19 FDA reports)
CHOLELITHIASIS ( 19 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 19 FDA reports)
EMOTIONAL DISORDER ( 19 FDA reports)
HAEMODYNAMIC INSTABILITY ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
METASTASES TO LUNG ( 19 FDA reports)
MUSCLE SPASMS ( 19 FDA reports)
OCULAR HYPERTENSION ( 19 FDA reports)
PNEUMONIA ASPIRATION ( 19 FDA reports)
SALIVARY HYPERSECRETION ( 19 FDA reports)
TONGUE INJURY ( 19 FDA reports)
ABSCESS JAW ( 18 FDA reports)
ACTINOMYCOSIS ( 18 FDA reports)
DENTAL FISTULA ( 18 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
HYPERTHERMIA MALIGNANT ( 18 FDA reports)
LEUKOENCEPHALOPATHY ( 18 FDA reports)
NODAL RHYTHM ( 18 FDA reports)
OESOPHAGITIS ULCERATIVE ( 18 FDA reports)
OSTEITIS ( 18 FDA reports)
PARALYSIS ( 18 FDA reports)
PARAPLEGIA ( 18 FDA reports)
PERIODONTAL DISEASE ( 18 FDA reports)
PRIMARY SEQUESTRUM ( 18 FDA reports)
PULMONARY HAEMORRHAGE ( 18 FDA reports)
RESTLESSNESS ( 18 FDA reports)
SINUS DISORDER ( 18 FDA reports)
TENDONITIS ( 18 FDA reports)
URINARY RETENTION ( 18 FDA reports)
WHEEZING ( 18 FDA reports)
AZOTAEMIA ( 17 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 17 FDA reports)
DERMATITIS ACNEIFORM ( 17 FDA reports)
EDENTULOUS ( 17 FDA reports)
JAW OPERATION ( 17 FDA reports)
LARYNGEAL OEDEMA ( 17 FDA reports)
LARYNGOSPASM ( 17 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 17 FDA reports)
MOVEMENT DISORDER ( 17 FDA reports)
MYALGIA ( 17 FDA reports)
NO THERAPEUTIC RESPONSE ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
SENSORY DISTURBANCE ( 17 FDA reports)
SOCIAL PROBLEM ( 17 FDA reports)
TREATMENT NONCOMPLIANCE ( 17 FDA reports)
VENTRICULAR HYPOKINESIA ( 17 FDA reports)
VISUAL ACUITY REDUCED ( 17 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 17 FDA reports)
ACCIDENTAL OVERDOSE ( 16 FDA reports)
CARDIAC MURMUR ( 16 FDA reports)
CEREBRAL ATROPHY ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 16 FDA reports)
FAMILY STRESS ( 16 FDA reports)
HAEMATOCRIT DECREASED ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 16 FDA reports)
HYPERLIPIDAEMIA ( 16 FDA reports)
LACERATION ( 16 FDA reports)
MITRAL VALVE CALCIFICATION ( 16 FDA reports)
MUSCLE DISORDER ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
OBESITY ( 16 FDA reports)
PRODUCT QUALITY ISSUE ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
PROTEINURIA ( 16 FDA reports)
PSYCHOTIC DISORDER ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
STRESS CARDIOMYOPATHY ( 16 FDA reports)
SURGERY ( 16 FDA reports)
TACHYPNOEA ( 16 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 16 FDA reports)
ABASIA ( 15 FDA reports)
ANOREXIA ( 15 FDA reports)
ASPIRATION ( 15 FDA reports)
ATRIAL FLUTTER ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 15 FDA reports)
COLONIC POLYP ( 15 FDA reports)
EJECTION FRACTION DECREASED ( 15 FDA reports)
HAEMODIALYSIS ( 15 FDA reports)
HEMIPARESIS ( 15 FDA reports)
JAUNDICE ( 15 FDA reports)
LYMPHADENOPATHY ( 15 FDA reports)
METASTASES TO LIVER ( 15 FDA reports)
OSTEONECROSIS ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
VERTIGO ( 15 FDA reports)
ACIDOSIS ( 14 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 14 FDA reports)
BLINDNESS UNILATERAL ( 14 FDA reports)
BRAIN DEATH ( 14 FDA reports)
BREAST CANCER METASTATIC ( 14 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 14 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 14 FDA reports)
DRY MOUTH ( 14 FDA reports)
DYSGEUSIA ( 14 FDA reports)
GENERALISED OEDEMA ( 14 FDA reports)
GINGIVITIS ( 14 FDA reports)
GOITRE ( 14 FDA reports)
GRAND MAL CONVULSION ( 14 FDA reports)
HALLUCINATION ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
ILL-DEFINED DISORDER ( 14 FDA reports)
INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
MECHANICAL VENTILATION ( 14 FDA reports)
OLIGURIA ( 14 FDA reports)
PANIC ATTACK ( 14 FDA reports)
PULSE ABSENT ( 14 FDA reports)
SEROTONIN SYNDROME ( 14 FDA reports)
SINUS ARREST ( 14 FDA reports)
SLEEP APNOEA SYNDROME ( 14 FDA reports)
SPEECH DISORDER ( 14 FDA reports)
TOOTH ABSCESS ( 14 FDA reports)
URTICARIA ( 14 FDA reports)
WHEELCHAIR USER ( 14 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 13 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 13 FDA reports)
AORTIC VALVE INCOMPETENCE ( 13 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 13 FDA reports)
ARTERIOSPASM CORONARY ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK ( 13 FDA reports)
BLINDNESS ( 13 FDA reports)
BONE DENSITY DECREASED ( 13 FDA reports)
DEFORMITY ( 13 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 13 FDA reports)
DIVERTICULUM INTESTINAL ( 13 FDA reports)
FAILURE TO THRIVE ( 13 FDA reports)
FLUID OVERLOAD ( 13 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 13 FDA reports)
LIFE EXPECTANCY SHORTENED ( 13 FDA reports)
LONG QT SYNDROME ( 13 FDA reports)
LUNG DISORDER ( 13 FDA reports)
MEDICATION ERROR ( 13 FDA reports)
NEPHROLITHIASIS ( 13 FDA reports)
OSTEOARTHRITIS ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
POLLAKIURIA ( 13 FDA reports)
PUPIL FIXED ( 13 FDA reports)
SCAR ( 13 FDA reports)
TYPE 2 DIABETES MELLITUS ( 13 FDA reports)
VERBAL ABUSE ( 13 FDA reports)
ACUTE PULMONARY OEDEMA ( 12 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
BLOOD UREA INCREASED ( 12 FDA reports)
CORONARY ARTERY BYPASS ( 12 FDA reports)
DECUBITUS ULCER ( 12 FDA reports)
ELECTROLYTE IMBALANCE ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 12 FDA reports)
HYPOTONIA ( 12 FDA reports)
HYPOVENTILATION ( 12 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 12 FDA reports)
IRIDOCYCLITIS ( 12 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 12 FDA reports)
LUNG INFILTRATION ( 12 FDA reports)
MEMORY IMPAIRMENT ( 12 FDA reports)
MENTAL IMPAIRMENT ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
METASTATIC NEOPLASM ( 12 FDA reports)
MUCOSAL INFLAMMATION ( 12 FDA reports)
ORTHOSTATIC HYPOTENSION ( 12 FDA reports)
OSTEOPOROSIS ( 12 FDA reports)
PHOTOPHOBIA ( 12 FDA reports)
RADICULOPATHY ( 12 FDA reports)
RASH PRURITIC ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
RENAL CYST ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
VENTRICULAR ARRHYTHMIA ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
AORTIC VALVE STENOSIS ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
CACHEXIA ( 11 FDA reports)
CARDIAC OUTPUT DECREASED ( 11 FDA reports)
CERVICAL SPINAL STENOSIS ( 11 FDA reports)
CHEST X-RAY ABNORMAL ( 11 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DYSPNOEA EXERTIONAL ( 11 FDA reports)
EMPHYSEMA ( 11 FDA reports)
FACE OEDEMA ( 11 FDA reports)
FLUID RETENTION ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HERPES SIMPLEX ( 11 FDA reports)
INFLAMMATION ( 11 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 11 FDA reports)
OESOPHAGITIS ( 11 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 11 FDA reports)
RENAL DISORDER ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
SPINAL COMPRESSION FRACTURE ( 11 FDA reports)
SPUTUM DISCOLOURED ( 11 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
TUMOUR LYSIS SYNDROME ( 11 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
ANTERIOR CHAMBER DISORDER ( 10 FDA reports)
ANTICHOLINERGIC SYNDROME ( 10 FDA reports)
AORTIC DISORDER ( 10 FDA reports)
APHASIA ( 10 FDA reports)
ARTHROPATHY ( 10 FDA reports)
ASPIRATION PLEURAL CAVITY ( 10 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
CARDIOVASCULAR DISORDER ( 10 FDA reports)
CEREBRAL ISCHAEMIA ( 10 FDA reports)
CHOLINERGIC SYNDROME ( 10 FDA reports)
CREPITATIONS ( 10 FDA reports)
DECREASED INTEREST ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
DRY SKIN ( 10 FDA reports)
EPISTAXIS ( 10 FDA reports)
FIBROSIS ( 10 FDA reports)
HEPATITIS ( 10 FDA reports)
HYDROCEPHALUS ( 10 FDA reports)
HYPOMAGNESAEMIA ( 10 FDA reports)
IRRITABILITY ( 10 FDA reports)
KLEBSIELLA INFECTION ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
LACUNAR INFARCTION ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
MUSCLE TWITCHING ( 10 FDA reports)
NASAL CONGESTION ( 10 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 10 FDA reports)
OSTEOPENIA ( 10 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 10 FDA reports)
PRESYNCOPE ( 10 FDA reports)
STOMATITIS ( 10 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 10 FDA reports)
SUICIDE ATTEMPT ( 10 FDA reports)
THROAT IRRITATION ( 10 FDA reports)
ULCERATIVE KERATITIS ( 10 FDA reports)
ADVERSE EVENT ( 9 FDA reports)
ANOXIC ENCEPHALOPATHY ( 9 FDA reports)
BLISTER ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
BONE MARROW FAILURE ( 9 FDA reports)
CATARACT OPERATION ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CEREBRAL HAEMATOMA ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
GLAUCOMA ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HAEMORRHOIDS ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HEPATOSPLENOMEGALY ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPOVOLAEMIA ( 9 FDA reports)
ILEUS ( 9 FDA reports)
ISCHAEMIA ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MIGRAINE ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
ORAL HERPES ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PLEURECTOMY ( 9 FDA reports)
PROCEDURAL HYPOTENSION ( 9 FDA reports)
PUPILS UNEQUAL ( 9 FDA reports)
RALES ( 9 FDA reports)
RASH MACULO-PAPULAR ( 9 FDA reports)
RHINITIS ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
SPLENOMEGALY ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
VENTRICULAR HYPERTROPHY ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
ANGINA UNSTABLE ( 8 FDA reports)
AORTIC VALVE CALCIFICATION ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
ASBESTOSIS ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 8 FDA reports)
BONE DEBRIDEMENT ( 8 FDA reports)
CARDIAC FAILURE ACUTE ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CAROTID ARTERY STENOSIS ( 8 FDA reports)
CATARACT ( 8 FDA reports)
CHEST TUBE INSERTION ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
COLITIS ISCHAEMIC ( 8 FDA reports)
CORONARY ARTERY STENOSIS ( 8 FDA reports)
DENTURE WEARER ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
ENDOPHTHALMITIS ( 8 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HEMIPLEGIA ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
INGROWING NAIL ( 8 FDA reports)
INJECTION SITE NECROSIS ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
INTERMITTENT CLAUDICATION ( 8 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 8 FDA reports)
MOUTH ULCERATION ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
ORTHOPNOEA ( 8 FDA reports)
PHARYNGEAL OEDEMA ( 8 FDA reports)
POST PROCEDURAL HAEMATOMA ( 8 FDA reports)
PRODUCTIVE COUGH ( 8 FDA reports)
PSYCHIATRIC SYMPTOM ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
THROAT TIGHTNESS ( 8 FDA reports)
TOOTH DISORDER ( 8 FDA reports)
URETERIC OBSTRUCTION ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 8 FDA reports)
WOUND DRAINAGE ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
AORTIC THROMBOSIS ( 7 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 7 FDA reports)
BLADDER OBSTRUCTION ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
BRAIN INJURY ( 7 FDA reports)
BRAIN OEDEMA ( 7 FDA reports)
BREAKTHROUGH PAIN ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
CHOLECYSTECTOMY ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
CHOLECYSTITIS INFECTIVE ( 7 FDA reports)
COLON CANCER ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
DRUG SCREEN POSITIVE ( 7 FDA reports)
EXPOSED BONE IN JAW ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
GINGIVAL ATROPHY ( 7 FDA reports)
GINGIVAL DISORDER ( 7 FDA reports)
GINGIVAL OEDEMA ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPHAEMA ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
HYPOKINESIA ( 7 FDA reports)
HYPOTHERMIA ( 7 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
INTENTION TREMOR ( 7 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
INTESTINAL PERFORATION ( 7 FDA reports)
ISCHAEMIC HEPATITIS ( 7 FDA reports)
LABORATORY TEST ABNORMAL ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LOWER LIMB FRACTURE ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
PANCREATIC ATROPHY ( 7 FDA reports)
PENILE OEDEMA ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PLEURAL DECORTICATION ( 7 FDA reports)
POISONING ( 7 FDA reports)
PROSTATE CANCER METASTATIC ( 7 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 7 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 7 FDA reports)
SPLEEN CONGESTION ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TROPONIN INCREASED ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
ACCIDENT ( 6 FDA reports)
ACCIDENTAL DEATH ( 6 FDA reports)
ACNE ( 6 FDA reports)
ADRENAL INSUFFICIENCY ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
ANGER ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
CAROTID BRUIT ( 6 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 6 FDA reports)
CHOKING SENSATION ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CRYING ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
EYE INFLAMMATION ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
GRANULOCYTOPENIA ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HYPERCAPNIA ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
INTESTINAL INFARCTION ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
ORGAN FAILURE ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PNEUMATOSIS INTESTINALIS ( 6 FDA reports)
POLYPECTOMY ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
RETINAL ARTERY OCCLUSION ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
SPINAL FRACTURE ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
URETERAL STENT INSERTION ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
WOUND DEHISCENCE ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
BILIARY SEPSIS ( 5 FDA reports)
BLOOD LACTIC ACID INCREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
CHEYNE-STOKES RESPIRATION ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
CORNEAL PERFORATION ( 5 FDA reports)
CORNEAL REFLEX DECREASED ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXOSTOSIS ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
FISTULA ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
GASTROINTESTINAL TOXICITY ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INGUINAL HERNIA ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LUNG CONSOLIDATION ( 5 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
MALLORY-WEISS SYNDROME ( 5 FDA reports)
MASTICATION DISORDER ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MULTIPLE SCLEROSIS ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
RESUSCITATION ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
SURGICAL PROCEDURE REPEATED ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
THORACOSTOMY ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
VITRECTOMY ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ASPERGER'S DISORDER ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BREATH ODOUR ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CHOROIDAL DETACHMENT ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DEVICE OCCLUSION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GLOBAL AMNESIA ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LUMBAR SPINAL STENOSIS ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
METAPLASIA ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYOCARDIAL FIBROSIS ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
NEONATAL HYPOTENSION ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OCULOGYRIC CRISIS ( 4 FDA reports)
OSTEOMA ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
PARVOVIRUS INFECTION ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PLEURAL ADHESION ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PURPURA ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
PYOGENIC GRANULOMA ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL FAILURE NEONATAL ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RETCHING ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RETINOPATHY OF PREMATURITY ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SNORING ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TERMINAL STATE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
VASOPLEGIA SYNDROME ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VENTRICULAR ASYSTOLE ( 4 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 4 FDA reports)
VITRITIS ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADNEXA UTERI CYST ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 3 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANAPHYLACTOID SHOCK ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
APATHY ( 3 FDA reports)
APHAKIA ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
BASOPHIL COUNT DECREASED ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD METHANOL INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CARDIOVERSION ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CEREBRAL HYPOPERFUSION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHOREOATHETOSIS ( 3 FDA reports)
CHOROIDITIS ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
CHYLOTHORAX ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CORONARY ARTERY PERFORATION ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CYSTOID MACULAR OEDEMA ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG EFFECT PROLONGED ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EUTHANASIA ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE INFECTION TOXOPLASMAL ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROENTERITIS BACTERIAL ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOTONY OF EYE ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
ILIAC ARTERY THROMBOSIS ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
ISCHAEMIC NEUROPATHY ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LARYNGEAL DYSPNOEA ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LYMPH NODE TUBERCULOSIS ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MACULAR FIBROSIS ( 3 FDA reports)
MACULAR SCAR ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 3 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUROMUSCULAR BLOCKADE ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERINEPHRIC COLLECTION ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 3 FDA reports)
PICKWICKIAN SYNDROME ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PNEUMOPERICARDIUM ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
RECTAL CANCER METASTATIC ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SEPSIS NEONATAL ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TOOTH IMPACTED ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
TRACHEAL OEDEMA ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WOUND ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADENOIDAL HYPERTROPHY ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE PROLAPSE ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL BIGEMINY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONTACT LENS COMPLICATION ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYST ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GARDNERELLA INFECTION ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
IRIDOCELE ( 2 FDA reports)
IRIS ADHESIONS ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEUKOSTASIS ( 2 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 2 FDA reports)
MASS ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTASES TO THORAX ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
MYOGLOBINAEMIA ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
MYOTONIC DYSTROPHY ( 2 FDA reports)
NASAL TURBINATE ABNORMALITY ( 2 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEONATAL ANURIA ( 2 FDA reports)
NEONATAL CARDIAC FAILURE ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROMYELITIS OPTICA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PIGMENT DISPERSION SYNDROME ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RADIATION FIBROSIS ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REGRESSIVE BEHAVIOUR ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SALMONELLA BACTERAEMIA ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STENT REMOVAL ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
ULCER ( 2 FDA reports)
UMBILICAL CORD PROLAPSE ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION INDUCED COMPLICATED ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALVEOLAR OSTEITIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION VASCULAR ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTERIOR CHAMBER FLARE ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE ATRESIA ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATELECTASIS NEONATAL ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BISPECTRAL INDEX DECREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CYANIDE INCREASED ( 1 FDA reports)
BLOOD ELASTASE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAPILLARY NAIL REFILL TEST ABNORMAL ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHOROIDAL EFFUSION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL ENDOTHELIITIS ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEEP BRAIN STIMULATION ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DESCEMET'S MEMBRANE DISORDER ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUCHENNE MUSCULAR DYSTROPHY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE NORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLAVOBACTERIUM INFECTION ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GIANT CELL EPULIS ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERNAL HERNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
IRIDODONESIS ( 1 FDA reports)
IRIS NEOVASCULARISATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOW INCOME ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENISCUS REMOVAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOTIC CORNEAL ULCER ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
MYOTONIA CONGENITA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEONATAL CANDIDA INFECTION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHAEOCHROMOCYTOMA CRISIS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYGLANDULAR AUTOIMMUNE SYNDROME TYPE II ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ECHINOCOCCIASIS ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCLERAL BUCKLING SURGERY ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY DECREASED ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

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