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

DYSPNOEA ( 245 FDA reports)
ASTHMA ( 164 FDA reports)
PNEUMONIA ( 141 FDA reports)
PAIN ( 121 FDA reports)
NAUSEA ( 104 FDA reports)
ANXIETY ( 103 FDA reports)
HEADACHE ( 96 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 95 FDA reports)
COUGH ( 90 FDA reports)
FATIGUE ( 90 FDA reports)
DRUG INEFFECTIVE ( 89 FDA reports)
DIZZINESS ( 85 FDA reports)
ARTHRALGIA ( 83 FDA reports)
FALL ( 81 FDA reports)
DEATH ( 79 FDA reports)
ASTHENIA ( 74 FDA reports)
PAIN IN EXTREMITY ( 74 FDA reports)
VOMITING ( 74 FDA reports)
OEDEMA PERIPHERAL ( 73 FDA reports)
PRODUCT QUALITY ISSUE ( 73 FDA reports)
DIARRHOEA ( 68 FDA reports)
CHEST PAIN ( 66 FDA reports)
BACK PAIN ( 60 FDA reports)
DEPRESSION ( 60 FDA reports)
INSOMNIA ( 58 FDA reports)
BRONCHITIS ( 53 FDA reports)
PYREXIA ( 53 FDA reports)
SINUSITIS ( 49 FDA reports)
HYPERTENSION ( 48 FDA reports)
HYPOAESTHESIA ( 48 FDA reports)
MALAISE ( 48 FDA reports)
ABDOMINAL PAIN ( 47 FDA reports)
OSTEONECROSIS OF JAW ( 47 FDA reports)
URINARY TRACT INFECTION ( 47 FDA reports)
MYOCARDIAL INFARCTION ( 46 FDA reports)
ATRIAL FIBRILLATION ( 45 FDA reports)
HYPOTENSION ( 45 FDA reports)
CONSTIPATION ( 42 FDA reports)
DYSPHAGIA ( 42 FDA reports)
OSTEOARTHRITIS ( 42 FDA reports)
WHEEZING ( 42 FDA reports)
FEELING ABNORMAL ( 41 FDA reports)
WEIGHT DECREASED ( 41 FDA reports)
ABDOMINAL PAIN UPPER ( 38 FDA reports)
GAIT DISTURBANCE ( 38 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 38 FDA reports)
INJECTION SITE PAIN ( 38 FDA reports)
CHEST DISCOMFORT ( 36 FDA reports)
INJURY ( 36 FDA reports)
NASOPHARYNGITIS ( 36 FDA reports)
BONE DISORDER ( 35 FDA reports)
EMPHYSEMA ( 35 FDA reports)
ANAEMIA ( 34 FDA reports)
CEREBROVASCULAR ACCIDENT ( 34 FDA reports)
CONDITION AGGRAVATED ( 34 FDA reports)
MUSCLE SPASMS ( 34 FDA reports)
MYALGIA ( 34 FDA reports)
PRURITUS ( 34 FDA reports)
ATELECTASIS ( 31 FDA reports)
DECREASED APPETITE ( 31 FDA reports)
DRY MOUTH ( 31 FDA reports)
HYPERSENSITIVITY ( 31 FDA reports)
INFECTION ( 31 FDA reports)
MUSCULOSKELETAL PAIN ( 31 FDA reports)
PLEURAL EFFUSION ( 31 FDA reports)
BLOOD PRESSURE INCREASED ( 30 FDA reports)
CHOLELITHIASIS ( 30 FDA reports)
PAIN IN JAW ( 30 FDA reports)
RASH ( 30 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 29 FDA reports)
PARAESTHESIA ( 29 FDA reports)
RESPIRATORY FAILURE ( 29 FDA reports)
THROMBOSIS ( 29 FDA reports)
DIABETES MELLITUS ( 28 FDA reports)
HAEMOGLOBIN DECREASED ( 28 FDA reports)
WEIGHT INCREASED ( 28 FDA reports)
CONTUSION ( 27 FDA reports)
DYSPHONIA ( 27 FDA reports)
EMOTIONAL DISTRESS ( 27 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 27 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
VISION BLURRED ( 27 FDA reports)
HIATUS HERNIA ( 26 FDA reports)
ARTHRITIS ( 25 FDA reports)
LUNG DISORDER ( 25 FDA reports)
TREMOR ( 25 FDA reports)
CATARACT ( 24 FDA reports)
DEHYDRATION ( 24 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
CHILLS ( 23 FDA reports)
CONFUSIONAL STATE ( 23 FDA reports)
CONVULSION ( 23 FDA reports)
DEEP VEIN THROMBOSIS ( 23 FDA reports)
PULMONARY EMBOLISM ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
SEPSIS ( 23 FDA reports)
SYNCOPE ( 23 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
CELLULITIS ( 22 FDA reports)
CORONARY ARTERY DISEASE ( 22 FDA reports)
ERYTHEMA ( 22 FDA reports)
OSTEOMYELITIS ( 22 FDA reports)
SOMNOLENCE ( 22 FDA reports)
SUICIDAL IDEATION ( 22 FDA reports)
ABDOMINAL DISCOMFORT ( 21 FDA reports)
BONE PAIN ( 21 FDA reports)
DECREASED INTEREST ( 21 FDA reports)
RIB FRACTURE ( 21 FDA reports)
ANHEDONIA ( 20 FDA reports)
DYSPEPSIA ( 20 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
HALLUCINATION ( 20 FDA reports)
HYPERHIDROSIS ( 20 FDA reports)
MUSCULAR WEAKNESS ( 20 FDA reports)
NEUROPATHY PERIPHERAL ( 20 FDA reports)
OROPHARYNGEAL PAIN ( 20 FDA reports)
RESPIRATORY DISTRESS ( 20 FDA reports)
URTICARIA ( 20 FDA reports)
ILL-DEFINED DISORDER ( 19 FDA reports)
CANDIDIASIS ( 18 FDA reports)
DYSGEUSIA ( 18 FDA reports)
EPISTAXIS ( 18 FDA reports)
HYPOXIA ( 18 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 18 FDA reports)
LUNG NEOPLASM ( 18 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 18 FDA reports)
SCAR ( 18 FDA reports)
SLEEP APNOEA SYNDROME ( 18 FDA reports)
SPINAL OSTEOARTHRITIS ( 18 FDA reports)
STAPHYLOCOCCAL INFECTION ( 18 FDA reports)
SWELLING ( 18 FDA reports)
VIRAL INFECTION ( 18 FDA reports)
AMNESIA ( 17 FDA reports)
BALANCE DISORDER ( 17 FDA reports)
CARDIAC DISORDER ( 17 FDA reports)
EXOSTOSIS ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
HYPOPHAGIA ( 17 FDA reports)
LUNG INFECTION ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
RHEUMATOID ARTHRITIS ( 17 FDA reports)
RHINORRHOEA ( 17 FDA reports)
CHOKING ( 16 FDA reports)
DENTAL CARIES ( 16 FDA reports)
HAEMATOCRIT DECREASED ( 16 FDA reports)
HYPERGLYCAEMIA ( 16 FDA reports)
JOINT SWELLING ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
METASTASES TO BONE ( 16 FDA reports)
MOBILITY DECREASED ( 16 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 16 FDA reports)
NASAL CONGESTION ( 16 FDA reports)
OSTEONECROSIS ( 16 FDA reports)
BLOOD GLUCOSE INCREASED ( 15 FDA reports)
COLONIC POLYP ( 15 FDA reports)
DEFORMITY ( 15 FDA reports)
DIVERTICULUM ( 15 FDA reports)
DRUG ADMINISTRATION ERROR ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
GASTRIC ULCER ( 15 FDA reports)
HYPERKALAEMIA ( 15 FDA reports)
RENAL DISORDER ( 15 FDA reports)
RESPIRATORY DISORDER ( 15 FDA reports)
ROTATOR CUFF SYNDROME ( 15 FDA reports)
SPINAL FRACTURE ( 15 FDA reports)
STOMATITIS ( 15 FDA reports)
THROAT TIGHTNESS ( 15 FDA reports)
TOOTH EXTRACTION ( 15 FDA reports)
TOOTH FRACTURE ( 15 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
DISCOMFORT ( 14 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 14 FDA reports)
FLATULENCE ( 14 FDA reports)
IMPAIRED HEALING ( 14 FDA reports)
INFLUENZA LIKE ILLNESS ( 14 FDA reports)
LUNG NEOPLASM MALIGNANT ( 14 FDA reports)
MENTAL STATUS CHANGES ( 14 FDA reports)
RESTLESS LEGS SYNDROME ( 14 FDA reports)
SLEEP DISORDER ( 14 FDA reports)
TOOTHACHE ( 14 FDA reports)
ACUTE RESPIRATORY FAILURE ( 13 FDA reports)
ADVERSE EVENT ( 13 FDA reports)
APHASIA ( 13 FDA reports)
BLOOD CREATININE INCREASED ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
HOT FLUSH ( 13 FDA reports)
HYPERKERATOSIS ( 13 FDA reports)
HYPOTHYROIDISM ( 13 FDA reports)
INJECTION SITE HAEMATOMA ( 13 FDA reports)
INJECTION SITE HAEMORRHAGE ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
MOVEMENT DISORDER ( 13 FDA reports)
NERVOUSNESS ( 13 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
PRODUCTIVE COUGH ( 13 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 13 FDA reports)
UNEVALUABLE EVENT ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
FISTULA ( 12 FDA reports)
GLAUCOMA ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
MACULAR DEGENERATION ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
MENTAL DISORDER ( 12 FDA reports)
MIGRAINE ( 12 FDA reports)
MITRAL VALVE INCOMPETENCE ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
RENAL FAILURE CHRONIC ( 12 FDA reports)
RESPIRATORY TRACT INFECTION ( 12 FDA reports)
SPINAL COLUMN STENOSIS ( 12 FDA reports)
STRESS ( 12 FDA reports)
SWELLING FACE ( 12 FDA reports)
THROAT IRRITATION ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
VERTIGO ( 12 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 12 FDA reports)
ABASIA ( 11 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
APHONIA ( 11 FDA reports)
ARTHROPATHY ( 11 FDA reports)
BRADYCARDIA ( 11 FDA reports)
CHOLECYSTITIS CHRONIC ( 11 FDA reports)
DRUG DOSE OMISSION ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
DYSPNOEA EXERTIONAL ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HAEMORRHOIDS ( 11 FDA reports)
HYPERLIPIDAEMIA ( 11 FDA reports)
ILEUS ( 11 FDA reports)
INFLAMMATION ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
PULMONARY CONGESTION ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
TOOTH DISORDER ( 11 FDA reports)
TREATMENT NONCOMPLIANCE ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
FACIAL PAIN ( 10 FDA reports)
FRACTURE ( 10 FDA reports)
GALLBLADDER DISORDER ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HEPATIC CYST ( 10 FDA reports)
INHALATION THERAPY ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
LIP SWELLING ( 10 FDA reports)
LYMPHADENOPATHY ( 10 FDA reports)
MASS ( 10 FDA reports)
MULTIPLE MYELOMA ( 10 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
ORAL PAIN ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PHARYNGEAL OEDEMA ( 10 FDA reports)
SCOLIOSIS ( 10 FDA reports)
SINUS TACHYCARDIA ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
ABNORMAL DREAMS ( 9 FDA reports)
AGITATION ( 9 FDA reports)
ANAPHYLACTIC REACTION ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
ATAXIA ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CARDIO-RESPIRATORY ARREST ( 9 FDA reports)
COLITIS ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DEPRESSED MOOD ( 9 FDA reports)
DIVERTICULUM INTESTINAL ( 9 FDA reports)
ECONOMIC PROBLEM ( 9 FDA reports)
EYE PAIN ( 9 FDA reports)
FOOT DEFORMITY ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HYPOCALCAEMIA ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 9 FDA reports)
KYPHOSIS ( 9 FDA reports)
LARYNGITIS ( 9 FDA reports)
LUMBAR SPINAL STENOSIS ( 9 FDA reports)
LUNG INFILTRATION ( 9 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 9 FDA reports)
MOUTH ULCERATION ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
RENAL CYST ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
UROSEPSIS ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 8 FDA reports)
BILIARY DILATATION ( 8 FDA reports)
BLOOD CALCIUM DECREASED ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BREAST CANCER ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
COMA ( 8 FDA reports)
COMPRESSION FRACTURE ( 8 FDA reports)
DENTAL FISTULA ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 8 FDA reports)
GOITRE ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
HAEMATOMA ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
INCONTINENCE ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
LARYNGEAL OEDEMA ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
METASTASES TO SPINE ( 8 FDA reports)
MOOD SWINGS ( 8 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 8 FDA reports)
NODULE ( 8 FDA reports)
NON-CARDIAC CHEST PAIN ( 8 FDA reports)
PERIODONTAL DISEASE ( 8 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
STRESS FRACTURE ( 8 FDA reports)
SURGERY ( 8 FDA reports)
SWOLLEN TONGUE ( 8 FDA reports)
UTERINE HAEMORRHAGE ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
AORTIC ANEURYSM ( 7 FDA reports)
ASTIGMATISM ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BLINDNESS TRANSIENT ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD MAGNESIUM DECREASED ( 7 FDA reports)
BONE LESION ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
CYST ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HEPATITIS C ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
MULTIPLE SCLEROSIS ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
NEOPLASM ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PULMONARY MASS ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
THROMBOCYTOSIS ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
ANGER ( 6 FDA reports)
ANGIOEDEMA ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
FACIAL BONES FRACTURE ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
FLUID OVERLOAD ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GOUT ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HOARSENESS ( 6 FDA reports)
HYPERMETROPIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
LIFE EXPECTANCY SHORTENED ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LOWER LIMB FRACTURE ( 6 FDA reports)
MULTIPLE INJURIES ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
MYOPIA ( 6 FDA reports)
NECK MASS ( 6 FDA reports)
NERVE INJURY ( 6 FDA reports)
OBESITY ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
RADICULOPATHY ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RETCHING ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
TRAUMATIC LUNG INJURY ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
WOUND ( 6 FDA reports)
ADNEXA UTERI MASS ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BONE DEBRIDEMENT ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CRYING ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DERMAL CYST ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
FEAR ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
KNEE ARTHROPLASTY ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
METASTASES TO LUNG ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
OTORRHOEA ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PERIODONTITIS ( 5 FDA reports)
PERONEAL NERVE PALSY ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
STOMATITIS NECROTISING ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TOOTH INFECTION ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASTEATOSIS ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD BILIRUBIN DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CHOROIDAL DETACHMENT ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ECTROPION ( 4 FDA reports)
EJECTION FRACTION ABNORMAL ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
EOSINOPHIL COUNT DECREASED ( 4 FDA reports)
ERB'S PALSY ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYE NAEVUS ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
FIBROMA ( 4 FDA reports)
GASTRINOMA ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
GLOBULINS INCREASED ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOMENORRHOEA ( 4 FDA reports)
HYPOTONY OF EYE ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
INTESTINAL POLYP ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LEFT ATRIAL DILATATION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIGAMENT RUPTURE ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MYELOMA RECURRENCE ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 4 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 4 FDA reports)
OESOPHAGEAL RUPTURE ( 4 FDA reports)
OPTIC NERVE CUPPING ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PLASMACYTOSIS ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
RADICULITIS LUMBOSACRAL ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RECTAL PROLAPSE ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
SNORING ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
VESICAL FISTULA ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABSCESS OF EYELID ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ASPIRATION JOINT ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST OEDEMA ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BURNOUT SYNDROME ( 3 FDA reports)
CALCIFICATION METASTATIC ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CUTIS LAXA ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DENTURE WEARER ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
FUSOBACTERIUM INFECTION ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GINGIVAL EROSION ( 3 FDA reports)
GINGIVAL OEDEMA ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HORDEOLUM ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 3 FDA reports)
INTRAOCULAR LENS IMPLANT ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEUKODYSTROPHY ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
NASAL ULCER ( 3 FDA reports)
NEURITIS ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERINEAL ABSCESS ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
SPONDYLOLYSIS ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACNE ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FULGURATION ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEITIS DEFORMANS ( 2 FDA reports)
OSTEOGENESIS IMPERFECTA ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYP ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STRUCK BY LIGHTNING ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
WRIST DEFORMITY ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANKLE DEFORMITY ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AURA ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BAND SENSATION ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BLADDER ABLATION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAECUM OPERATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLOT RETRACTION TIME SHORTENED ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLPOSCOPY ABNORMAL ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL OESOPHAGEAL ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DEFORMITY ACQUIRED ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE THROMBOSIS ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTATIC CARCINOID TUMOUR ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSTEOARTHROPATHY ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURECTOMY ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPIROMETRY ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THREATENED LABOUR ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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