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

DYSPNOEA ( 332 FDA reports)
DRUG INEFFECTIVE ( 246 FDA reports)
PNEUMONIA ( 235 FDA reports)
PAIN ( 200 FDA reports)
NAUSEA ( 190 FDA reports)
ASTHMA ( 179 FDA reports)
DIZZINESS ( 161 FDA reports)
ANXIETY ( 155 FDA reports)
VOMITING ( 150 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 145 FDA reports)
CHEST PAIN ( 139 FDA reports)
FATIGUE ( 138 FDA reports)
HEADACHE ( 127 FDA reports)
HYPOTENSION ( 127 FDA reports)
OEDEMA PERIPHERAL ( 121 FDA reports)
PYREXIA ( 121 FDA reports)
DEPRESSION ( 120 FDA reports)
ANAEMIA ( 117 FDA reports)
COUGH ( 113 FDA reports)
DIARRHOEA ( 113 FDA reports)
ASTHENIA ( 111 FDA reports)
FALL ( 102 FDA reports)
BACK PAIN ( 100 FDA reports)
BRONCHITIS ( 98 FDA reports)
INJURY ( 94 FDA reports)
MALAISE ( 94 FDA reports)
RESPIRATORY FAILURE ( 90 FDA reports)
PAIN IN EXTREMITY ( 86 FDA reports)
DEHYDRATION ( 84 FDA reports)
CONDITION AGGRAVATED ( 82 FDA reports)
URINARY TRACT INFECTION ( 82 FDA reports)
ARTHRALGIA ( 81 FDA reports)
HYPERSENSITIVITY ( 80 FDA reports)
PLEURAL EFFUSION ( 80 FDA reports)
DEEP VEIN THROMBOSIS ( 79 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 77 FDA reports)
HYPERTENSION ( 76 FDA reports)
RENAL FAILURE ACUTE ( 76 FDA reports)
WEIGHT DECREASED ( 76 FDA reports)
RENAL FAILURE ( 69 FDA reports)
CONVULSION ( 68 FDA reports)
WHEEZING ( 68 FDA reports)
TREMOR ( 67 FDA reports)
INSOMNIA ( 65 FDA reports)
OSTEONECROSIS OF JAW ( 65 FDA reports)
ABDOMINAL PAIN ( 64 FDA reports)
HYPOAESTHESIA ( 64 FDA reports)
PARAESTHESIA ( 64 FDA reports)
TACHYCARDIA ( 64 FDA reports)
DEATH ( 63 FDA reports)
MYOCARDIAL INFARCTION ( 63 FDA reports)
GAIT DISTURBANCE ( 59 FDA reports)
ATRIAL FIBRILLATION ( 58 FDA reports)
CEREBROVASCULAR ACCIDENT ( 58 FDA reports)
OSTEOARTHRITIS ( 58 FDA reports)
PULMONARY EMBOLISM ( 58 FDA reports)
CARDIAC ARREST ( 57 FDA reports)
HAEMOGLOBIN DECREASED ( 57 FDA reports)
HEART RATE INCREASED ( 56 FDA reports)
RASH ( 56 FDA reports)
SYNCOPE ( 56 FDA reports)
CONFUSIONAL STATE ( 55 FDA reports)
DYSPHAGIA ( 55 FDA reports)
FEELING ABNORMAL ( 55 FDA reports)
RESPIRATORY DISTRESS ( 55 FDA reports)
THROMBOCYTOPENIA ( 55 FDA reports)
URTICARIA ( 53 FDA reports)
CELLULITIS ( 52 FDA reports)
CHILLS ( 52 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 52 FDA reports)
SINUSITIS ( 52 FDA reports)
BLOOD CREATININE INCREASED ( 51 FDA reports)
HALLUCINATION ( 51 FDA reports)
CONSTIPATION ( 50 FDA reports)
HYPERHIDROSIS ( 50 FDA reports)
LOSS OF CONSCIOUSNESS ( 50 FDA reports)
DYSGEUSIA ( 48 FDA reports)
HAEMATURIA ( 48 FDA reports)
HYPOKALAEMIA ( 48 FDA reports)
MYALGIA ( 48 FDA reports)
ABDOMINAL PAIN UPPER ( 47 FDA reports)
VISION BLURRED ( 47 FDA reports)
LACTIC ACIDOSIS ( 46 FDA reports)
DECREASED APPETITE ( 45 FDA reports)
HYPOXIA ( 45 FDA reports)
MUSCLE SPASMS ( 45 FDA reports)
MUSCULAR WEAKNESS ( 45 FDA reports)
PALPITATIONS ( 45 FDA reports)
ANHEDONIA ( 44 FDA reports)
CATARACT ( 44 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 44 FDA reports)
CHEST DISCOMFORT ( 43 FDA reports)
NEUTROPENIA ( 43 FDA reports)
WEIGHT INCREASED ( 43 FDA reports)
ABDOMINAL DISTENSION ( 42 FDA reports)
BLOOD GLUCOSE INCREASED ( 42 FDA reports)
BLOOD PRESSURE INCREASED ( 42 FDA reports)
HYPERLIPIDAEMIA ( 42 FDA reports)
HYPONATRAEMIA ( 42 FDA reports)
CONTUSION ( 41 FDA reports)
DIABETES MELLITUS ( 41 FDA reports)
DRUG INTERACTION ( 41 FDA reports)
LYMPHADENOPATHY ( 41 FDA reports)
OVERDOSE ( 41 FDA reports)
SEPSIS ( 41 FDA reports)
UNRESPONSIVE TO STIMULI ( 41 FDA reports)
VERTIGO ( 41 FDA reports)
RENAL FAILURE CHRONIC ( 40 FDA reports)
BONE PAIN ( 39 FDA reports)
NASOPHARYNGITIS ( 39 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 39 FDA reports)
PULMONARY OEDEMA ( 39 FDA reports)
THROAT IRRITATION ( 39 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 38 FDA reports)
PRURITUS ( 38 FDA reports)
SINUS TACHYCARDIA ( 38 FDA reports)
BRONCHOSPASM ( 37 FDA reports)
NEOPLASM MALIGNANT ( 37 FDA reports)
PANCYTOPENIA ( 37 FDA reports)
SPINAL OSTEOARTHRITIS ( 37 FDA reports)
STAPHYLOCOCCAL INFECTION ( 37 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 36 FDA reports)
MENTAL STATUS CHANGES ( 36 FDA reports)
VISUAL IMPAIRMENT ( 36 FDA reports)
EMOTIONAL DISTRESS ( 35 FDA reports)
METABOLIC ACIDOSIS ( 35 FDA reports)
METASTASES TO BONE ( 35 FDA reports)
DRUG HYPERSENSITIVITY ( 34 FDA reports)
HIATUS HERNIA ( 34 FDA reports)
BONE DISORDER ( 33 FDA reports)
ERYTHEMA ( 33 FDA reports)
OXYGEN SATURATION DECREASED ( 33 FDA reports)
VENTRICULAR TACHYCARDIA ( 33 FDA reports)
EPISTAXIS ( 32 FDA reports)
INFECTION ( 32 FDA reports)
OEDEMA ( 32 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 32 FDA reports)
DRY MOUTH ( 31 FDA reports)
HAEMATOCRIT DECREASED ( 31 FDA reports)
HERPES ZOSTER ( 31 FDA reports)
NEUROPATHY PERIPHERAL ( 31 FDA reports)
OESOPHAGITIS ( 31 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 30 FDA reports)
ADVERSE DRUG REACTION ( 30 FDA reports)
CARDIAC FAILURE ( 30 FDA reports)
LEUKOPENIA ( 30 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 29 FDA reports)
ANAPHYLACTIC REACTION ( 29 FDA reports)
BRADYCARDIA ( 29 FDA reports)
BURNING SENSATION ( 29 FDA reports)
CARDIAC DISORDER ( 29 FDA reports)
DYSPHONIA ( 29 FDA reports)
EMPHYSEMA ( 29 FDA reports)
HAEMORRHAGE ( 29 FDA reports)
OSTEONECROSIS ( 29 FDA reports)
OSTEOPOROSIS ( 29 FDA reports)
PLATELET COUNT DECREASED ( 29 FDA reports)
TOOTHACHE ( 29 FDA reports)
URINARY RETENTION ( 29 FDA reports)
ACUTE RESPIRATORY FAILURE ( 28 FDA reports)
ATELECTASIS ( 28 FDA reports)
DYSURIA ( 28 FDA reports)
IMPAIRED HEALING ( 28 FDA reports)
IRRITABILITY ( 28 FDA reports)
MEMORY IMPAIRMENT ( 28 FDA reports)
MITRAL VALVE INCOMPETENCE ( 28 FDA reports)
OSTEOMYELITIS ( 28 FDA reports)
PAIN IN JAW ( 28 FDA reports)
STOMATITIS ( 28 FDA reports)
SWELLING ( 28 FDA reports)
TOOTH LOSS ( 28 FDA reports)
CHOLELITHIASIS ( 27 FDA reports)
HAEMATOCHEZIA ( 27 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 27 FDA reports)
SOMNOLENCE ( 27 FDA reports)
SUICIDAL IDEATION ( 27 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 27 FDA reports)
ANGINA PECTORIS ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 26 FDA reports)
LUNG NEOPLASM MALIGNANT ( 26 FDA reports)
TYPE 2 DIABETES MELLITUS ( 26 FDA reports)
ARTHRITIS ( 25 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 25 FDA reports)
PRODUCT QUALITY ISSUE ( 25 FDA reports)
RECTAL HAEMORRHAGE ( 25 FDA reports)
RENAL CYST ( 25 FDA reports)
ASPIRATION ( 24 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
DISTURBANCE IN ATTENTION ( 24 FDA reports)
METASTASES TO LIVER ( 24 FDA reports)
OROPHARYNGEAL PAIN ( 24 FDA reports)
SWELLING FACE ( 24 FDA reports)
AGGRESSION ( 23 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
DEFORMITY ( 23 FDA reports)
HAEMATOMA ( 23 FDA reports)
HEART RATE DECREASED ( 23 FDA reports)
HYPERGLYCAEMIA ( 23 FDA reports)
HYPOGLYCAEMIA ( 23 FDA reports)
LETHARGY ( 23 FDA reports)
LEUKOCYTOSIS ( 23 FDA reports)
MIGRAINE ( 23 FDA reports)
OSTEOPENIA ( 23 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 23 FDA reports)
ARRHYTHMIA ( 22 FDA reports)
DIPLOPIA ( 22 FDA reports)
DRUG EFFECT DECREASED ( 22 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 22 FDA reports)
RHABDOMYOLYSIS ( 22 FDA reports)
SPEECH DISORDER ( 22 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 22 FDA reports)
CORONARY ARTERY DISEASE ( 21 FDA reports)
ESSENTIAL HYPERTENSION ( 21 FDA reports)
EYE SWELLING ( 21 FDA reports)
GLAUCOMA ( 21 FDA reports)
MUSCULOSKELETAL PAIN ( 21 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 21 FDA reports)
NASAL CONGESTION ( 21 FDA reports)
NECK PAIN ( 21 FDA reports)
STRESS ( 21 FDA reports)
AGITATION ( 20 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 20 FDA reports)
AMNESIA ( 20 FDA reports)
DYSPEPSIA ( 20 FDA reports)
FACIAL BONES FRACTURE ( 20 FDA reports)
FLUID OVERLOAD ( 20 FDA reports)
FLUSHING ( 20 FDA reports)
HEPATIC LESION ( 20 FDA reports)
HOT FLUSH ( 20 FDA reports)
HYPOTHYROIDISM ( 20 FDA reports)
LUNG NEOPLASM ( 20 FDA reports)
MULTI-ORGAN FAILURE ( 20 FDA reports)
NERVOUSNESS ( 20 FDA reports)
TOOTH DISORDER ( 20 FDA reports)
ABNORMAL BEHAVIOUR ( 19 FDA reports)
DISORIENTATION ( 19 FDA reports)
DIVERTICULITIS ( 19 FDA reports)
DYSPNOEA EXERTIONAL ( 19 FDA reports)
EYE PAIN ( 19 FDA reports)
INCORRECT DOSE ADMINISTERED ( 19 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
ORAL CANDIDIASIS ( 19 FDA reports)
PATHOLOGICAL FRACTURE ( 19 FDA reports)
PRODUCTIVE COUGH ( 19 FDA reports)
STATUS ASTHMATICUS ( 19 FDA reports)
SUDDEN DEATH ( 19 FDA reports)
ABDOMINAL DISCOMFORT ( 18 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 18 FDA reports)
EATING DISORDER ( 18 FDA reports)
ENCEPHALOPATHY ( 18 FDA reports)
GANGRENE ( 18 FDA reports)
GOUT ( 18 FDA reports)
HAEMATEMESIS ( 18 FDA reports)
INJECTION SITE ERYTHEMA ( 18 FDA reports)
PANCREATITIS ( 18 FDA reports)
PHARYNGEAL OEDEMA ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
SCOLIOSIS ( 18 FDA reports)
SKIN ULCER ( 18 FDA reports)
SWOLLEN TONGUE ( 18 FDA reports)
VITAMIN D DEFICIENCY ( 18 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 17 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 17 FDA reports)
BLISTER ( 17 FDA reports)
BLOOD POTASSIUM DECREASED ( 17 FDA reports)
BONE LESION ( 17 FDA reports)
CARDIO-RESPIRATORY ARREST ( 17 FDA reports)
CARDIOMYOPATHY ( 17 FDA reports)
COAGULOPATHY ( 17 FDA reports)
COMA ( 17 FDA reports)
FIBROMYALGIA ( 17 FDA reports)
GASTRITIS ( 17 FDA reports)
HIP FRACTURE ( 17 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
MALNUTRITION ( 17 FDA reports)
MEDICATION ERROR ( 17 FDA reports)
SKIN DISCOLOURATION ( 17 FDA reports)
SPINAL FRACTURE ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 17 FDA reports)
THYROID NEOPLASM ( 17 FDA reports)
TREATMENT NONCOMPLIANCE ( 17 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 16 FDA reports)
ALOPECIA ( 16 FDA reports)
ANOREXIA ( 16 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 16 FDA reports)
CANDIDIASIS ( 16 FDA reports)
CARDIAC MURMUR ( 16 FDA reports)
CHOLECYSTITIS CHRONIC ( 16 FDA reports)
CIRCULATORY COLLAPSE ( 16 FDA reports)
COGNITIVE DISORDER ( 16 FDA reports)
CYST ( 16 FDA reports)
DIVERTICULUM ( 16 FDA reports)
DRUG ADMINISTRATION ERROR ( 16 FDA reports)
ENTEROCOCCAL INFECTION ( 16 FDA reports)
FUNGAL INFECTION ( 16 FDA reports)
GASTRIC ULCER ( 16 FDA reports)
HAEMORRHOIDS ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
HYDRONEPHROSIS ( 16 FDA reports)
INJECTION SITE HAEMORRHAGE ( 16 FDA reports)
INJECTION SITE PAIN ( 16 FDA reports)
LIVER DISORDER ( 16 FDA reports)
MACULAR DEGENERATION ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 16 FDA reports)
MULTIPLE MYELOMA ( 16 FDA reports)
OBESITY ( 16 FDA reports)
OFF LABEL USE ( 16 FDA reports)
RENAL DISORDER ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
THYROID CANCER ( 16 FDA reports)
TOOTH INFECTION ( 16 FDA reports)
URINARY INCONTINENCE ( 16 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
CARDIOGENIC SHOCK ( 15 FDA reports)
CERUMEN IMPACTION ( 15 FDA reports)
CYANOSIS ( 15 FDA reports)
ECZEMA ( 15 FDA reports)
EYE DISORDER ( 15 FDA reports)
FLUID RETENTION ( 15 FDA reports)
FOOT FRACTURE ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
INJECTION SITE HAEMATOMA ( 15 FDA reports)
LACERATION ( 15 FDA reports)
MOBILITY DECREASED ( 15 FDA reports)
MYOSITIS ( 15 FDA reports)
NIGHTMARE ( 15 FDA reports)
ORAL PAIN ( 15 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
WEIGHT FLUCTUATION ( 15 FDA reports)
ABASIA ( 14 FDA reports)
AORTIC ANEURYSM ( 14 FDA reports)
ARTERIOSCLEROSIS ( 14 FDA reports)
ATAXIA ( 14 FDA reports)
AZOTAEMIA ( 14 FDA reports)
BREAST CANCER RECURRENT ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
CHRONIC SINUSITIS ( 14 FDA reports)
DYSKINESIA ( 14 FDA reports)
GINGIVAL BLEEDING ( 14 FDA reports)
HAEMOPTYSIS ( 14 FDA reports)
HYPOVOLAEMIA ( 14 FDA reports)
JOINT SWELLING ( 14 FDA reports)
NEPHROLITHIASIS ( 14 FDA reports)
OCULAR HYPERAEMIA ( 14 FDA reports)
ORAL DISORDER ( 14 FDA reports)
ORTHOSTATIC HYPOTENSION ( 14 FDA reports)
OTITIS MEDIA ( 14 FDA reports)
PERICARDIAL EFFUSION ( 14 FDA reports)
PERIPHERAL COLDNESS ( 14 FDA reports)
PREMATURE BABY ( 14 FDA reports)
PRIMARY SEQUESTRUM ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
STRABISMUS ( 14 FDA reports)
THROAT TIGHTNESS ( 14 FDA reports)
ABDOMINAL HERNIA ( 13 FDA reports)
ADVERSE EVENT ( 13 FDA reports)
ANURIA ( 13 FDA reports)
BLOOD GLUCOSE DECREASED ( 13 FDA reports)
BRUXISM ( 13 FDA reports)
CAESAREAN SECTION ( 13 FDA reports)
ESCHERICHIA INFECTION ( 13 FDA reports)
GINGIVAL PAIN ( 13 FDA reports)
HEART RATE IRREGULAR ( 13 FDA reports)
INFLUENZA LIKE ILLNESS ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 13 FDA reports)
MENINGIOMA ( 13 FDA reports)
METASTASES TO LUNG ( 13 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 13 FDA reports)
PANIC ATTACK ( 13 FDA reports)
PNEUMOTHORAX ( 13 FDA reports)
PSYCHOTIC DISORDER ( 13 FDA reports)
PULMONARY CONGESTION ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
RHEUMATOID ARTHRITIS ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
BLADDER DISORDER ( 12 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 12 FDA reports)
BLOOD UREA INCREASED ( 12 FDA reports)
BODY HEIGHT DECREASED ( 12 FDA reports)
BREAST CANCER ( 12 FDA reports)
BRONCHOSTENOSIS ( 12 FDA reports)
COLD SWEAT ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
DRUG DEPENDENCE ( 12 FDA reports)
DRUG INTOLERANCE ( 12 FDA reports)
EAR PAIN ( 12 FDA reports)
FEBRILE NEUTROPENIA ( 12 FDA reports)
HYPERCHOLESTEROLAEMIA ( 12 FDA reports)
KIDNEY SMALL ( 12 FDA reports)
METASTASES TO SPINE ( 12 FDA reports)
MOUTH ULCERATION ( 12 FDA reports)
NOCTURIA ( 12 FDA reports)
PALLOR ( 12 FDA reports)
PNEUMONITIS ( 12 FDA reports)
RHINORRHOEA ( 12 FDA reports)
RIB FRACTURE ( 12 FDA reports)
SLEEP APNOEA SYNDROME ( 12 FDA reports)
SQUAMOUS CELL CARCINOMA ( 12 FDA reports)
SUBDURAL HAEMATOMA ( 12 FDA reports)
THROMBOPHLEBITIS ( 12 FDA reports)
TOOTH ABSCESS ( 12 FDA reports)
VENTRICULAR HYPERTROPHY ( 12 FDA reports)
APPENDICITIS ( 11 FDA reports)
ARTHROPATHY ( 11 FDA reports)
ASCITES ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 11 FDA reports)
BLOOD ALBUMIN DECREASED ( 11 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 11 FDA reports)
BREATH ODOUR ( 11 FDA reports)
CHEILITIS ( 11 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 11 FDA reports)
CULTURE URINE POSITIVE ( 11 FDA reports)
CYSTITIS ( 11 FDA reports)
DECUBITUS ULCER ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 11 FDA reports)
DIVERTICULUM INTESTINAL ( 11 FDA reports)
GALLBLADDER DISORDER ( 11 FDA reports)
GASTROINTESTINAL DISORDER ( 11 FDA reports)
GENERALISED OEDEMA ( 11 FDA reports)
IMPAIRED DRIVING ABILITY ( 11 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 11 FDA reports)
LEUKAEMIA ( 11 FDA reports)
LUNG INFECTION ( 11 FDA reports)
MIXED DEAFNESS ( 11 FDA reports)
MOVEMENT DISORDER ( 11 FDA reports)
MULTIPLE FRACTURES ( 11 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 11 FDA reports)
POLLAKIURIA ( 11 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
RENAL ATROPHY ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
RESTLESSNESS ( 11 FDA reports)
RHINITIS ALLERGIC ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
SPINAL COLUMN STENOSIS ( 11 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 11 FDA reports)
UNEVALUABLE EVENT ( 11 FDA reports)
ABDOMINAL PAIN LOWER ( 10 FDA reports)
ABNORMAL DREAMS ( 10 FDA reports)
ADVERSE REACTION ( 10 FDA reports)
BACK INJURY ( 10 FDA reports)
BACTEROIDES TEST POSITIVE ( 10 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 10 FDA reports)
BLOOD CALCIUM DECREASED ( 10 FDA reports)
BREAST MASS ( 10 FDA reports)
CAROTID ARTERY DISEASE ( 10 FDA reports)
CARPAL TUNNEL SYNDROME ( 10 FDA reports)
CELLULITIS ORBITAL ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
COLONIC POLYP ( 10 FDA reports)
DEAFNESS ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
EAR INFECTION ( 10 FDA reports)
GINGIVAL SWELLING ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
HEPATITIS ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 10 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
INJECTION SITE REACTION ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
INTESTINAL ISCHAEMIA ( 10 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 10 FDA reports)
LOCAL SWELLING ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
MUSCLE CRAMP ( 10 FDA reports)
OEDEMA MOUTH ( 10 FDA reports)
ORAL DISCOMFORT ( 10 FDA reports)
PERIODONTAL DISEASE ( 10 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 10 FDA reports)
PHLEBITIS ( 10 FDA reports)
PHYSICAL DISABILITY ( 10 FDA reports)
PROTEIN URINE ( 10 FDA reports)
PROTHROMBIN TIME PROLONGED ( 10 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 10 FDA reports)
RESPIRATORY TRACT OEDEMA ( 10 FDA reports)
SINUS BRADYCARDIA ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
ADRENAL MASS ( 9 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
BLADDER CANCER ( 9 FDA reports)
BLOOD PH DECREASED ( 9 FDA reports)
BONE FISSURE ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
COLPOCELE ( 9 FDA reports)
CONJUNCTIVITIS ( 9 FDA reports)
CRYING ( 9 FDA reports)
CYSTOSCOPY ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 9 FDA reports)
FOETAL GROWTH RETARDATION ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
HERPES VIRUS INFECTION ( 9 FDA reports)
HYDROCELE ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
INFECTED SKIN ULCER ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
MUCOSAL INFLAMMATION ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NEUROPATHIC ULCER ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
OSTEOMA ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
POOR PERIPHERAL CIRCULATION ( 9 FDA reports)
POST HERPETIC NEURALGIA ( 9 FDA reports)
PRESYNCOPE ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
RESTLESS LEGS SYNDROME ( 9 FDA reports)
SCREAMING ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
SPINAL COLUMN INJURY ( 9 FDA reports)
STRESS URINARY INCONTINENCE ( 9 FDA reports)
SUICIDE ATTEMPT ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
VAGINAL PROLAPSE ( 9 FDA reports)
VASCULITIS ( 9 FDA reports)
WRIST FRACTURE ( 9 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
ACUTE CORONARY SYNDROME ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ATROPHY ( 8 FDA reports)
BLOOD MAGNESIUM DECREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BREAST DISCHARGE ( 8 FDA reports)
BRONCHITIS CHRONIC ( 8 FDA reports)
CARDIOVASCULAR DISORDER ( 8 FDA reports)
CATHETER SITE HAEMORRHAGE ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
CHOKING ( 8 FDA reports)
COLITIS ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DEMENTIA ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
DRUG ABUSER ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
EMOTIONAL DISORDER ( 8 FDA reports)
ENDOCARDITIS ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
EUPHORIC MOOD ( 8 FDA reports)
EYE IRRITATION ( 8 FDA reports)
FEELING JITTERY ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
GASTRIC DISORDER ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
GLOSSODYNIA ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
ILEUS ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
LIMB INJURY ( 8 FDA reports)
MASTOIDITIS ( 8 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 8 FDA reports)
METASTASES TO SPLEEN ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
PRURITUS GENERALISED ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
SCIATICA ( 8 FDA reports)
TRANSPLANT FAILURE ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
VAGINAL INFECTION ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
AGRANULOCYTOSIS ( 7 FDA reports)
ANGER ( 7 FDA reports)
AORTIC VALVE SCLEROSIS ( 7 FDA reports)
BIPOLAR DISORDER ( 7 FDA reports)
BLINDNESS TRANSIENT ( 7 FDA reports)
BLOOD CALCIUM INCREASED ( 7 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
BRONCHOSPASM PARADOXICAL ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 7 FDA reports)
CONJUNCTIVAL OEDEMA ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
EMBOLISM VENOUS ( 7 FDA reports)
EYE MOVEMENT DISORDER ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
FEMUR FRACTURE ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
FOOT DEFORMITY ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HYPERKERATOSIS ( 7 FDA reports)
HYPERREFLEXIA ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
JUGULAR VEIN THROMBOSIS ( 7 FDA reports)
LIGAMENT SPRAIN ( 7 FDA reports)
MASTITIS ( 7 FDA reports)
MENISCUS LESION ( 7 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
MYOPATHY ( 7 FDA reports)
NEURALGIA ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
OVERWEIGHT ( 7 FDA reports)
PELVIC PAIN ( 7 FDA reports)
PREGNANCY ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
RALES ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
ACIDOSIS ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
APHONIA ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ATONIC SEIZURES ( 6 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BONE NEOPLASM MALIGNANT ( 6 FDA reports)
BREAST PAIN ( 6 FDA reports)
CALCULUS URETERIC ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
DISCOMFORT ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FISTULA ( 6 FDA reports)
FOETAL HEART RATE ABNORMAL ( 6 FDA reports)
GASTRIC PERFORATION ( 6 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 6 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 6 FDA reports)
GRAFT DYSFUNCTION ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAND FRACTURE ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HEPATITIS C ( 6 FDA reports)
HEPATOMEGALY ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
INJECTION SITE SWELLING ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
LEARNING DISABILITY ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LOBAR PNEUMONIA ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MANIA ( 6 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
NASAL TURBINATE ABNORMALITY ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
OESOPHAGITIS ULCERATIVE ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
ONYCHOLYSIS ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
ORAL TORUS ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
QUALITY OF LIFE DECREASED ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
SELF-MEDICATION ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
STRIDOR ( 6 FDA reports)
SYNOVITIS ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
THIRST ( 6 FDA reports)
TRISMUS ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VOCAL CORD PARALYSIS ( 6 FDA reports)
VOMITING PROJECTILE ( 6 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANION GAP INCREASED ( 5 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLADDER NECK OPERATION ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLINDNESS UNILATERAL ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CERVICAL SPINAL STENOSIS ( 5 FDA reports)
CLONUS ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COLON ADENOMA ( 5 FDA reports)
CONGENITAL BLADDER ANOMALY ( 5 FDA reports)
CORNEAL OPERATION ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
CYSTOPEXY ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 5 FDA reports)
DEVICE RELATED SEPSIS ( 5 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
EPIDURAL LIPOMATOSIS ( 5 FDA reports)
ERUCTATION ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEAR ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
GASTRECTOMY ( 5 FDA reports)
GASTRIC CANCER RECURRENT ( 5 FDA reports)
GASTRITIS ATROPHIC ( 5 FDA reports)
GASTROINTESTINAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
HYPOSPADIAS ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
INTRAOCULAR LENS IMPLANT ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
LEG AMPUTATION ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LUMBAR SPINAL STENOSIS ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MASS ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NECK MASS ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NODULE ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
OBSTRUCTION GASTRIC ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OPEN REDUCTION OF FRACTURE ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PARATHYROIDECTOMY ( 5 FDA reports)
PERIPHERAL NERVE INJURY ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
POSTOPERATIVE ILEUS ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
SCROTAL CYST ( 5 FDA reports)
SENSATION OF FOREIGN BODY ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SKULL MALFORMATION ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
STEATORRHOEA ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TRIGEMINAL NEURALGIA ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
VITAMIN B12 DEFICIENCY ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
WOUND ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACNE ( 4 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CATHETER PLACEMENT ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CHOREA ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DERMATITIS DIAPER ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ESCHERICHIA TEST POSITIVE ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GINGIVAL EROSION ( 4 FDA reports)
GINGIVAL OEDEMA ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOACUSIS ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOTONIC URINARY BLADDER ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INHALATION THERAPY ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
KIDNEY MALFORMATION ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LENTIGO ( 4 FDA reports)
LEUKAEMOID REACTION ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LISTLESS ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LUNG HYPERINFLATION ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUROPATHY ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERIRECTAL ABSCESS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PLATELET ADHESIVENESS DECREASED ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
RADICULOPATHY ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
REGURGITATION OF FOOD ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RETCHING ( 4 FDA reports)
RHONCHI ( 4 FDA reports)
SCAR ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SLEEP TALKING ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SOFT TISSUE INJURY ( 4 FDA reports)
SOMNAMBULISM ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
SPINAL DECOMPRESSION ( 4 FDA reports)
SPINAL LAMINECTOMY ( 4 FDA reports)
STEM CELL TRANSPLANT ( 4 FDA reports)
SURGERY ( 4 FDA reports)
TALIPES ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TONIC CLONIC MOVEMENTS ( 4 FDA reports)
TOOTH DEPOSIT ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
VAGOTOMY ( 4 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 4 FDA reports)
VERTEBRAL WEDGING ( 4 FDA reports)
VIRAL PHARYNGITIS ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
WOUND SECRETION ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APNOEA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD IRON INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CATECHOLAMINES URINE INCREASED ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONGENITAL CYSTIC LUNG ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EXECUTIVE DYSFUNCTION ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GINGIVAL ERYTHEMA ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INFUSION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MESENTERIC PANNICULITIS ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POLYP ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SERRATIA INFECTION ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STRABISMUS CONGENITAL ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY SEDIMENT ABNORMAL ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID DECREASED ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADENOIDAL HYPERTROPHY ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTISM ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLADDER AGENESIS ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBELLAR TUMOUR ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 2 FDA reports)
CONGENITAL NOSE MALFORMATION ( 2 FDA reports)
CRANIAL SUTURES WIDENING ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENDOMETRIAL DISORDER ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FIBRIN INCREASED ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FORCEPS DELIVERY ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GROWING PAINS ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPNAGOGIC HALLUCINATION ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MECONIUM STAIN ( 2 FDA reports)
MELAS SYNDROME ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLICA SYNDROME ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYGLANDULAR DISORDER ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL AGENESIS ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENILE OSTEOPOROSIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINGLE UMBILICAL ARTERY ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STATUS MIGRAINOSUS ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE AMYLASE INCREASED ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
WANDERING PACEMAKER ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
YAWNING ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE DECREASED ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY NEONATAL ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNIOCENTESIS ABNORMAL ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AVERSION ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLEPHARAL PIGMENTATION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CANDIDA NAPPY RASH ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHILDHOOD PSYCHOSIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTIC FIBROSIS LUNG ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DOUBLE URETER ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ENCEPHALITIS ALLERGIC ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FEAR OF PREGNANCY ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPOCALCIURIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEAL GANGRENE ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE SCAR ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
KWASHIORKOR ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL CYST ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL PH ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST VACCINATION SYNDROME ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA NEONATAL ( 1 FDA reports)
PULMONARY SEQUESTRATION ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELECTIVE IGA IMMUNODEFICIENCY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERRATIA BACTERAEMIA ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STARING ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TIC ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE MERCURY ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINITIS ATROPHIC ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)

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