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

DYSPNOEA ( 867 FDA reports)
DRUG INEFFECTIVE ( 782 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 611 FDA reports)
ASTHMA ( 499 FDA reports)
COUGH ( 338 FDA reports)
DYSPHONIA ( 330 FDA reports)
PNEUMONIA ( 300 FDA reports)
DEATH ( 299 FDA reports)
NAUSEA ( 255 FDA reports)
DIZZINESS ( 238 FDA reports)
PAIN ( 233 FDA reports)
FATIGUE ( 227 FDA reports)
HEADACHE ( 211 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 205 FDA reports)
CHEST PAIN ( 190 FDA reports)
ANXIETY ( 179 FDA reports)
ASTHENIA ( 161 FDA reports)
VOMITING ( 160 FDA reports)
BRONCHITIS ( 147 FDA reports)
WHEEZING ( 143 FDA reports)
WEIGHT INCREASED ( 142 FDA reports)
ARTHRALGIA ( 136 FDA reports)
PRODUCT QUALITY ISSUE ( 136 FDA reports)
OEDEMA PERIPHERAL ( 135 FDA reports)
PAIN IN EXTREMITY ( 131 FDA reports)
PRURITUS ( 130 FDA reports)
DIARRHOEA ( 128 FDA reports)
MALAISE ( 126 FDA reports)
CHEST DISCOMFORT ( 125 FDA reports)
FALL ( 125 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 114 FDA reports)
TREMOR ( 114 FDA reports)
DEPRESSION ( 110 FDA reports)
HEART RATE INCREASED ( 110 FDA reports)
CANDIDIASIS ( 109 FDA reports)
MYOCARDIAL INFARCTION ( 109 FDA reports)
WEIGHT DECREASED ( 109 FDA reports)
HYPERSENSITIVITY ( 108 FDA reports)
HYPOTENSION ( 107 FDA reports)
RASH ( 107 FDA reports)
INSOMNIA ( 106 FDA reports)
PYREXIA ( 106 FDA reports)
PALPITATIONS ( 104 FDA reports)
FEELING ABNORMAL ( 102 FDA reports)
HYPERTENSION ( 102 FDA reports)
CONDITION AGGRAVATED ( 101 FDA reports)
DIABETES MELLITUS ( 100 FDA reports)
MUSCLE SPASMS ( 98 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 97 FDA reports)
BACK PAIN ( 96 FDA reports)
RESPIRATORY FAILURE ( 94 FDA reports)
ATRIAL FIBRILLATION ( 93 FDA reports)
INJURY ( 92 FDA reports)
BLOOD GLUCOSE INCREASED ( 88 FDA reports)
DRY MOUTH ( 88 FDA reports)
BLOOD PRESSURE INCREASED ( 87 FDA reports)
DEHYDRATION ( 84 FDA reports)
CATARACT ( 83 FDA reports)
ORAL CANDIDIASIS ( 81 FDA reports)
ABDOMINAL PAIN ( 80 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 80 FDA reports)
THROAT IRRITATION ( 80 FDA reports)
ANAEMIA ( 79 FDA reports)
URINARY TRACT INFECTION ( 78 FDA reports)
VISION BLURRED ( 77 FDA reports)
CONSTIPATION ( 75 FDA reports)
DYSPHAGIA ( 75 FDA reports)
FLUSHING ( 75 FDA reports)
URTICARIA ( 73 FDA reports)
ILL-DEFINED DISORDER ( 72 FDA reports)
DYSGEUSIA ( 71 FDA reports)
EPISTAXIS ( 71 FDA reports)
ERYTHEMA ( 70 FDA reports)
LOSS OF CONSCIOUSNESS ( 70 FDA reports)
OVERDOSE ( 70 FDA reports)
APHONIA ( 69 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 65 FDA reports)
MYALGIA ( 65 FDA reports)
RENAL FAILURE ACUTE ( 65 FDA reports)
HYPOAESTHESIA ( 60 FDA reports)
GAIT DISTURBANCE ( 59 FDA reports)
SINUSITIS ( 59 FDA reports)
CONFUSIONAL STATE ( 58 FDA reports)
PARAESTHESIA ( 58 FDA reports)
SUICIDAL IDEATION ( 58 FDA reports)
ABDOMINAL PAIN UPPER ( 56 FDA reports)
CARDIAC ARREST ( 56 FDA reports)
PULMONARY EMBOLISM ( 56 FDA reports)
CEREBROVASCULAR ACCIDENT ( 55 FDA reports)
SOMNOLENCE ( 55 FDA reports)
CONVULSION ( 54 FDA reports)
ECONOMIC PROBLEM ( 53 FDA reports)
MEMORY IMPAIRMENT ( 53 FDA reports)
NASOPHARYNGITIS ( 52 FDA reports)
NERVOUSNESS ( 52 FDA reports)
TACHYCARDIA ( 52 FDA reports)
CARDIO-RESPIRATORY ARREST ( 51 FDA reports)
HYPERHIDROSIS ( 51 FDA reports)
CARDIAC DISORDER ( 50 FDA reports)
CONTUSION ( 50 FDA reports)
HOARSENESS ( 50 FDA reports)
ADVERSE EVENT ( 48 FDA reports)
HAEMOGLOBIN DECREASED ( 48 FDA reports)
RENAL FAILURE ( 48 FDA reports)
TYPE 2 DIABETES MELLITUS ( 48 FDA reports)
ANAPHYLACTIC REACTION ( 47 FDA reports)
RESPIRATORY DISTRESS ( 47 FDA reports)
SYNCOPE ( 47 FDA reports)
SWELLING FACE ( 46 FDA reports)
ANHEDONIA ( 45 FDA reports)
DYSPEPSIA ( 45 FDA reports)
EMOTIONAL DISTRESS ( 45 FDA reports)
MUSCULAR WEAKNESS ( 45 FDA reports)
CHILLS ( 43 FDA reports)
DECREASED APPETITE ( 43 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 43 FDA reports)
OROPHARYNGEAL PAIN ( 42 FDA reports)
STATUS ASTHMATICUS ( 42 FDA reports)
BRONCHOSPASM ( 41 FDA reports)
HYPERGLYCAEMIA ( 41 FDA reports)
HYPOXIA ( 41 FDA reports)
LUNG DISORDER ( 41 FDA reports)
MEDICATION ERROR ( 41 FDA reports)
PRODUCTIVE COUGH ( 41 FDA reports)
ABASIA ( 40 FDA reports)
SEPSIS ( 40 FDA reports)
STOMATITIS ( 40 FDA reports)
SWELLING ( 40 FDA reports)
VISUAL IMPAIRMENT ( 40 FDA reports)
PLEURAL EFFUSION ( 39 FDA reports)
GLAUCOMA ( 38 FDA reports)
INFECTION ( 38 FDA reports)
ALOPECIA ( 37 FDA reports)
DYSPNOEA EXERTIONAL ( 37 FDA reports)
RESPIRATORY DISORDER ( 37 FDA reports)
THROAT TIGHTNESS ( 37 FDA reports)
IRRITABILITY ( 36 FDA reports)
MITRAL VALVE INCOMPETENCE ( 36 FDA reports)
RESPIRATORY ARREST ( 36 FDA reports)
AGITATION ( 35 FDA reports)
BLOOD PRESSURE DECREASED ( 35 FDA reports)
CHOKING ( 35 FDA reports)
FEMUR FRACTURE ( 35 FDA reports)
INFLUENZA LIKE ILLNESS ( 35 FDA reports)
LARYNGITIS ( 35 FDA reports)
MUSCULOSKELETAL PAIN ( 35 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 35 FDA reports)
AGGRESSION ( 34 FDA reports)
DRUG INTERACTION ( 34 FDA reports)
HEART RATE IRREGULAR ( 34 FDA reports)
OSTEOARTHRITIS ( 34 FDA reports)
STRESS ( 34 FDA reports)
ANGINA PECTORIS ( 33 FDA reports)
ARRHYTHMIA ( 33 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 33 FDA reports)
BONE DISORDER ( 33 FDA reports)
CHOLELITHIASIS ( 33 FDA reports)
ABDOMINAL DISCOMFORT ( 32 FDA reports)
INCORRECT DOSE ADMINISTERED ( 32 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 32 FDA reports)
SWOLLEN TONGUE ( 32 FDA reports)
UNEVALUABLE EVENT ( 32 FDA reports)
DRUG ADMINISTRATION ERROR ( 31 FDA reports)
EMPHYSEMA ( 31 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 31 FDA reports)
MENTAL STATUS CHANGES ( 31 FDA reports)
OXYGEN SATURATION DECREASED ( 31 FDA reports)
ABDOMINAL DISTENSION ( 30 FDA reports)
AGEUSIA ( 30 FDA reports)
BALANCE DISORDER ( 30 FDA reports)
CELLULITIS ( 30 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 30 FDA reports)
MIGRAINE ( 30 FDA reports)
NEUROPATHY PERIPHERAL ( 30 FDA reports)
NEUTROPENIA ( 30 FDA reports)
ORAL FUNGAL INFECTION ( 30 FDA reports)
PHARYNGEAL OEDEMA ( 30 FDA reports)
SPEECH DISORDER ( 30 FDA reports)
BRADYCARDIA ( 29 FDA reports)
DEEP VEIN THROMBOSIS ( 29 FDA reports)
GLOSSODYNIA ( 29 FDA reports)
MULTIPLE INJURIES ( 29 FDA reports)
OEDEMA ( 29 FDA reports)
THROMBOCYTOPENIA ( 29 FDA reports)
BLOOD CREATININE INCREASED ( 28 FDA reports)
FEAR ( 28 FDA reports)
NASAL CONGESTION ( 28 FDA reports)
ORAL PAIN ( 28 FDA reports)
PULMONARY CONGESTION ( 28 FDA reports)
PULMONARY HYPERTENSION ( 28 FDA reports)
RECTAL HAEMORRHAGE ( 28 FDA reports)
ABNORMAL DREAMS ( 27 FDA reports)
ANOREXIA ( 27 FDA reports)
ATELECTASIS ( 27 FDA reports)
BONE PAIN ( 27 FDA reports)
CORONARY ARTERY DISEASE ( 27 FDA reports)
DISORIENTATION ( 27 FDA reports)
FEELING HOT ( 27 FDA reports)
MOUTH ULCERATION ( 27 FDA reports)
NECK PAIN ( 27 FDA reports)
OSTEONECROSIS ( 27 FDA reports)
PULMONARY OEDEMA ( 27 FDA reports)
TOOTH EXTRACTION ( 27 FDA reports)
ACUTE RESPIRATORY FAILURE ( 26 FDA reports)
CARDIAC FAILURE ( 26 FDA reports)
DISEASE PROGRESSION ( 26 FDA reports)
HAEMORRHAGE ( 26 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 25 FDA reports)
DRY SKIN ( 25 FDA reports)
FUNGAL INFECTION ( 25 FDA reports)
OSTEOPOROSIS ( 25 FDA reports)
PANCREATITIS ( 25 FDA reports)
RENAL FAILURE CHRONIC ( 25 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 25 FDA reports)
TREATMENT NONCOMPLIANCE ( 25 FDA reports)
ADVERSE DRUG REACTION ( 24 FDA reports)
ANGER ( 24 FDA reports)
ANOXIC ENCEPHALOPATHY ( 24 FDA reports)
DYSURIA ( 24 FDA reports)
EYE PAIN ( 24 FDA reports)
HERPES ZOSTER ( 24 FDA reports)
JOINT SWELLING ( 24 FDA reports)
MENTAL DISORDER ( 24 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 24 FDA reports)
STRESS FRACTURE ( 24 FDA reports)
ABNORMAL BEHAVIOUR ( 23 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 23 FDA reports)
DRUG DOSE OMISSION ( 23 FDA reports)
FEELING JITTERY ( 23 FDA reports)
HYPONATRAEMIA ( 23 FDA reports)
SUICIDE ATTEMPT ( 23 FDA reports)
AMNESIA ( 22 FDA reports)
ARTHRITIS ( 22 FDA reports)
CARDIOMEGALY ( 22 FDA reports)
DRUG HYPERSENSITIVITY ( 22 FDA reports)
DRY THROAT ( 22 FDA reports)
EMOTIONAL DISORDER ( 22 FDA reports)
HYPERACUSIS ( 22 FDA reports)
MOBILITY DECREASED ( 22 FDA reports)
OFF LABEL USE ( 22 FDA reports)
SLEEP APNOEA SYNDROME ( 22 FDA reports)
TOOTH DISORDER ( 22 FDA reports)
VISUAL ACUITY REDUCED ( 22 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 22 FDA reports)
BLINDNESS ( 21 FDA reports)
BLINDNESS TRANSIENT ( 21 FDA reports)
DEAFNESS TRANSITORY ( 21 FDA reports)
DENTAL CARIES ( 21 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
LETHARGY ( 21 FDA reports)
THROMBOSIS ( 21 FDA reports)
TONGUE DISORDER ( 21 FDA reports)
ANOSMIA ( 20 FDA reports)
BURNING SENSATION ( 20 FDA reports)
HAEMOPTYSIS ( 20 FDA reports)
HALLUCINATION ( 20 FDA reports)
HOT FLUSH ( 20 FDA reports)
MULTI-ORGAN FAILURE ( 20 FDA reports)
PAIN IN JAW ( 20 FDA reports)
APHASIA ( 19 FDA reports)
DIABETIC NEUROPATHY ( 19 FDA reports)
DIPLOPIA ( 19 FDA reports)
DRUG EFFECT DECREASED ( 19 FDA reports)
GASTRIC DISORDER ( 19 FDA reports)
HYPOKALAEMIA ( 19 FDA reports)
IMPAIRED HEALING ( 19 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 19 FDA reports)
LUNG INFECTION ( 19 FDA reports)
PRESYNCOPE ( 19 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 19 FDA reports)
ANGIOEDEMA ( 18 FDA reports)
BLOOD GLUCOSE DECREASED ( 18 FDA reports)
DISTURBANCE IN ATTENTION ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
HAEMATOCHEZIA ( 18 FDA reports)
LUNG HYPERINFLATION ( 18 FDA reports)
NIGHTMARE ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
RASH PRURITIC ( 18 FDA reports)
RESTLESSNESS ( 18 FDA reports)
RHINORRHOEA ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
SURGERY ( 18 FDA reports)
TOOTH LOSS ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 17 FDA reports)
ATRIAL FLUTTER ( 17 FDA reports)
ATRIAL SEPTAL DEFECT ( 17 FDA reports)
BLOOD POTASSIUM DECREASED ( 17 FDA reports)
FLATULENCE ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
INFLUENZA ( 17 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 17 FDA reports)
LUNG NEOPLASM MALIGNANT ( 17 FDA reports)
LYMPHADENOPATHY ( 17 FDA reports)
OSTEOMYELITIS ( 17 FDA reports)
SKIN EXFOLIATION ( 17 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 17 FDA reports)
CYSTITIS ( 16 FDA reports)
DRY EYE ( 16 FDA reports)
EAR PAIN ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
HAEMATOCRIT DECREASED ( 16 FDA reports)
HAEMORRHOIDS ( 16 FDA reports)
HYPERSOMNIA ( 16 FDA reports)
HYPOVOLAEMIA ( 16 FDA reports)
LIP SWELLING ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 16 FDA reports)
LOBAR PNEUMONIA ( 16 FDA reports)
MYOCARDIAL ISCHAEMIA ( 16 FDA reports)
OSTEOPENIA ( 16 FDA reports)
PANIC ATTACK ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
PRURITUS GENERALISED ( 16 FDA reports)
RESPIRATORY TRACT CONGESTION ( 16 FDA reports)
RETCHING ( 16 FDA reports)
URINARY RETENTION ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
CARDIOMYOPATHY ( 15 FDA reports)
CHOKING SENSATION ( 15 FDA reports)
DEPRESSED MOOD ( 15 FDA reports)
EYE DISORDER ( 15 FDA reports)
EYE SWELLING ( 15 FDA reports)
EYELID PTOSIS ( 15 FDA reports)
FLUID RETENTION ( 15 FDA reports)
FRACTURE DISPLACEMENT ( 15 FDA reports)
HEPATIC ENZYME INCREASED ( 15 FDA reports)
HIATUS HERNIA ( 15 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 15 FDA reports)
MOVEMENT DISORDER ( 15 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 15 FDA reports)
POLLAKIURIA ( 15 FDA reports)
RHEUMATOID ARTHRITIS ( 15 FDA reports)
TOOTH FRACTURE ( 15 FDA reports)
TOOTHACHE ( 15 FDA reports)
VIRAL INFECTION ( 15 FDA reports)
BLOOD UREA INCREASED ( 14 FDA reports)
BURSITIS ( 14 FDA reports)
CARDIAC MURMUR ( 14 FDA reports)
COAGULOPATHY ( 14 FDA reports)
CRYING ( 14 FDA reports)
DISCOMFORT ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
HYPOTHYROIDISM ( 14 FDA reports)
JOINT STIFFNESS ( 14 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 14 FDA reports)
MOOD ALTERED ( 14 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 14 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
SKIN LACERATION ( 14 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 14 FDA reports)
VENTRICULAR FIBRILLATION ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
BLOOD SODIUM DECREASED ( 13 FDA reports)
CATARACT OPERATION ( 13 FDA reports)
GINGIVAL PAIN ( 13 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 13 FDA reports)
HOSPITALISATION ( 13 FDA reports)
INFUSION RELATED REACTION ( 13 FDA reports)
INJECTION SITE PAIN ( 13 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 13 FDA reports)
LEUKOPENIA ( 13 FDA reports)
LOCAL SWELLING ( 13 FDA reports)
LUNG INFILTRATION ( 13 FDA reports)
MACULAR DEGENERATION ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
NIGHT SWEATS ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
RENAL DISORDER ( 13 FDA reports)
RHINITIS ALLERGIC ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
SHOCK ( 13 FDA reports)
SKIN INDURATION ( 13 FDA reports)
SPUTUM DISCOLOURED ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
STREPTOCOCCAL INFECTION ( 13 FDA reports)
TONGUE DISCOLOURATION ( 13 FDA reports)
UNDERDOSE ( 13 FDA reports)
ACCIDENTAL OVERDOSE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLISTER ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 12 FDA reports)
COMPLETED SUICIDE ( 12 FDA reports)
DYSSTASIA ( 12 FDA reports)
EYE IRRITATION ( 12 FDA reports)
GRAND MAL CONVULSION ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
HIP FRACTURE ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 12 FDA reports)
MIDDLE INSOMNIA ( 12 FDA reports)
MUSCLE TIGHTNESS ( 12 FDA reports)
OEDEMA MOUTH ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
ACNE ( 11 FDA reports)
AFFECTIVE DISORDER ( 11 FDA reports)
BONE DEBRIDEMENT ( 11 FDA reports)
CARPAL TUNNEL SYNDROME ( 11 FDA reports)
CHOLECYSTITIS ACUTE ( 11 FDA reports)
COGNITIVE DISORDER ( 11 FDA reports)
COMA ( 11 FDA reports)
CYANOSIS ( 11 FDA reports)
DEFORMITY ( 11 FDA reports)
DIVERTICULITIS ( 11 FDA reports)
DIVERTICULUM ( 11 FDA reports)
EAR INFECTION ( 11 FDA reports)
EATING DISORDER ( 11 FDA reports)
ECZEMA ( 11 FDA reports)
EXCORIATION ( 11 FDA reports)
EXOSTOSIS ( 11 FDA reports)
EYE PRURITUS ( 11 FDA reports)
FOOT FRACTURE ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HYPOALBUMINAEMIA ( 11 FDA reports)
HYPOCALCAEMIA ( 11 FDA reports)
HYPOPHAGIA ( 11 FDA reports)
LIMB INJURY ( 11 FDA reports)
LOCALISED INFECTION ( 11 FDA reports)
PANCREATITIS CHRONIC ( 11 FDA reports)
PATHOLOGICAL FRACTURE ( 11 FDA reports)
PHARYNGITIS ( 11 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 11 FDA reports)
PSYCHOTIC DISORDER ( 11 FDA reports)
PULMONARY FIBROSIS ( 11 FDA reports)
RESTLESS LEGS SYNDROME ( 11 FDA reports)
SCAR ( 11 FDA reports)
SINUS TACHYCARDIA ( 11 FDA reports)
SKIN BURNING SENSATION ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
SUFFOCATION FEELING ( 11 FDA reports)
TACHYPNOEA ( 11 FDA reports)
TENDERNESS ( 11 FDA reports)
TINNITUS ( 11 FDA reports)
VOCAL CORD DISORDER ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
ARRESTED LABOUR ( 10 FDA reports)
ARTHROPATHY ( 10 FDA reports)
BRONCHOPNEUMONIA ( 10 FDA reports)
CAESAREAN SECTION ( 10 FDA reports)
DECREASED INTEREST ( 10 FDA reports)
DIASTOLIC DYSFUNCTION ( 10 FDA reports)
DYSKINESIA ( 10 FDA reports)
EXPIRED DRUG ADMINISTERED ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
GASTROENTERITIS VIRAL ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
HEPATITIS C ( 10 FDA reports)
HYPERLIPIDAEMIA ( 10 FDA reports)
HYPOAESTHESIA ORAL ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
JOINT CONTRACTURE ( 10 FDA reports)
MANIA ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
OBESITY ( 10 FDA reports)
ORAL DISCOMFORT ( 10 FDA reports)
ORAL SURGERY ( 10 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 10 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 10 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 10 FDA reports)
POOR QUALITY SLEEP ( 10 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 10 FDA reports)
SENSATION OF FOREIGN BODY ( 10 FDA reports)
SKIN DISORDER ( 10 FDA reports)
SPINAL OSTEOARTHRITIS ( 10 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 10 FDA reports)
VENTRICULAR HYPOKINESIA ( 10 FDA reports)
ADRENAL INSUFFICIENCY ( 9 FDA reports)
AORTIC VALVE INCOMPETENCE ( 9 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
AURICULAR SWELLING ( 9 FDA reports)
BACTERIAL INFECTION ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD CALCIUM DECREASED ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CHROMATURIA ( 9 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 9 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 9 FDA reports)
COELIAC DISEASE ( 9 FDA reports)
COLITIS ( 9 FDA reports)
COLONIC POLYP ( 9 FDA reports)
COMMINUTED FRACTURE ( 9 FDA reports)
CORONARY ARTERY STENOSIS ( 9 FDA reports)
CROHN'S DISEASE ( 9 FDA reports)
DELUSION ( 9 FDA reports)
DEVELOPMENTAL DELAY ( 9 FDA reports)
DEVICE MALFUNCTION ( 9 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
ERECTILE DYSFUNCTION ( 9 FDA reports)
FAMILY STRESS ( 9 FDA reports)
FEBRILE NEUTROPENIA ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
FRACTURE ( 9 FDA reports)
GINGIVAL INFECTION ( 9 FDA reports)
GINGIVAL SWELLING ( 9 FDA reports)
INJECTION SITE ERYTHEMA ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MELAENA ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
MULTIPLE MYELOMA ( 9 FDA reports)
MUSCLE CRAMP ( 9 FDA reports)
MUSCLE TWITCHING ( 9 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 9 FDA reports)
NERVE COMPRESSION ( 9 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PHARYNGEAL DISORDER ( 9 FDA reports)
PLEURITIC PAIN ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
PULMONARY MASS ( 9 FDA reports)
RASH MACULAR ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
SINUS DISORDER ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
SKIN TIGHTNESS ( 9 FDA reports)
SOCIAL PROBLEM ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
TOOTH DISCOLOURATION ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
VAGINAL HAEMORRHAGE ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
ABSCESS ( 8 FDA reports)
ACUTE SINUSITIS ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
CUSHINGOID ( 8 FDA reports)
CYST ( 8 FDA reports)
DRUG INTOLERANCE ( 8 FDA reports)
DRUG PRESCRIBING ERROR ( 8 FDA reports)
DRUG SCREEN POSITIVE ( 8 FDA reports)
FAECAL INCONTINENCE ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
HALLUCINATION, VISUAL ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HOMICIDAL IDEATION ( 8 FDA reports)
HYPERCHOLESTEROLAEMIA ( 8 FDA reports)
INHALATION THERAPY ( 8 FDA reports)
INJECTION SITE HAEMATOMA ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
JOINT DISLOCATION ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LUNG NEOPLASM ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
MULTIPLE SCLEROSIS ( 8 FDA reports)
MYASTHENIA GRAVIS ( 8 FDA reports)
MYOPATHY ( 8 FDA reports)
NON-CARDIAC CHEST PAIN ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
OROPHARYNGITIS FUNGAL ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PELVIC PAIN ( 8 FDA reports)
PERSONALITY CHANGE ( 8 FDA reports)
PRODUCT TASTE ABNORMAL ( 8 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
RENAL TUBULAR NECROSIS ( 8 FDA reports)
SKIN ATROPHY ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
STENT PLACEMENT ( 8 FDA reports)
STOMACH DISCOMFORT ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
THYROID DISORDER ( 8 FDA reports)
TOXIC ENCEPHALOPATHY ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
VERTIGO POSITIONAL ( 8 FDA reports)
VISUAL DISTURBANCE ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ANAEMIA POSTOPERATIVE ( 7 FDA reports)
ANKLE FRACTURE ( 7 FDA reports)
APHTHOUS STOMATITIS ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BRAIN DEATH ( 7 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 7 FDA reports)
CERVICAL SPINAL STENOSIS ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DIABETIC KETOACIDOSIS ( 7 FDA reports)
DILATATION VENTRICULAR ( 7 FDA reports)
DISABILITY ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
EJACULATION FAILURE ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
FEAR OF DEATH ( 7 FDA reports)
FEELING OF DESPAIR ( 7 FDA reports)
FRACTURE NONUNION ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
GOUT ( 7 FDA reports)
GROWTH RETARDATION ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCREASED APPETITE ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
ISCHAEMIA ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
LIGAMENT RUPTURE ( 7 FDA reports)
MAJOR DEPRESSION ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
NEURAL TUBE DEFECT ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 7 FDA reports)
OESOPHAGITIS ( 7 FDA reports)
ORAL INFECTION ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 7 FDA reports)
QUALITY OF LIFE DECREASED ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
RESPIRATORY TRACT IRRITATION ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SHOULDER ARTHROPLASTY ( 7 FDA reports)
SINUS HEADACHE ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SKIN FIBROSIS ( 7 FDA reports)
SKIN HYPERTROPHY ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
SPINA BIFIDA ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
THYROIDECTOMY ( 7 FDA reports)
TOOTH INFECTION ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
URINE ANALYSIS ABNORMAL ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
ABORTION SPONTANEOUS ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
BEDRIDDEN ( 6 FDA reports)
BIOPSY ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BREAST CANCER ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DEVICE FAILURE ( 6 FDA reports)
DIABETIC RETINOPATHY ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
EJECTION FRACTION DECREASED ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
FACIAL PAIN ( 6 FDA reports)
FALLOT'S TETRALOGY ( 6 FDA reports)
FRACTURE DELAYED UNION ( 6 FDA reports)
FRUSTRATION ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GINGIVAL DISORDER ( 6 FDA reports)
GINGIVAL RECESSION ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
HEART RATE ABNORMAL ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPERMETROPIA ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 6 FDA reports)
LACRIMATION INCREASED ( 6 FDA reports)
LIMB ASYMMETRY ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MASS ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MENINGOMYELOCELE ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 6 FDA reports)
PROSTATOMEGALY ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
PULMONARY ARTERY ATRESIA ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 6 FDA reports)
RADICULOPATHY ( 6 FDA reports)
RIGHT VENTRICULAR FAILURE ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
SPINAL COMPRESSION FRACTURE ( 6 FDA reports)
TALIPES ( 6 FDA reports)
TOBACCO USER ( 6 FDA reports)
TOOTH REPAIR ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 5 FDA reports)
ALVEOLOPLASTY ( 5 FDA reports)
APNOEA ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BREAST PAIN ( 5 FDA reports)
BREATH ODOUR ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BULLOUS LUNG DISEASE ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 5 FDA reports)
CRANIOTOMY ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DENTAL FISTULA ( 5 FDA reports)
DEVICE INEFFECTIVE ( 5 FDA reports)
DIZZINESS POSTURAL ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FOOT DEFORMITY ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GINGIVAL ERYTHEMA ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAND FRACTURE ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LUNG CONSOLIDATION ( 5 FDA reports)
MASTICATION DISORDER ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MOUTH PLAQUE ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
MYODESOPSIA ( 5 FDA reports)
NASOPHARYNGEAL DISORDER ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NOCTURIA ( 5 FDA reports)
NODULE ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PHARYNGEAL ERYTHEMA ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PRESBYOPIA ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RALES ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SELF-INJURIOUS IDEATION ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SLUGGISHNESS ( 5 FDA reports)
SUDDEN ONSET OF SLEEP ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
TENSION ( 5 FDA reports)
THIRST ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
TONGUE ULCERATION ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 5 FDA reports)
VERTEBRAL INJURY ( 5 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
WOUND ( 5 FDA reports)
WOUND DRAINAGE ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BENIGN CARDIAC NEOPLASM ( 4 FDA reports)
BIOPSY LUNG ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC FIBROMA ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
COLLAPSE OF LUNG ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONGENITAL TRACHEOMALACIA ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DENTURE WEARER ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DEXTROCARDIA ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
EAR DISCOMFORT ( 4 FDA reports)
ECHOCARDIOGRAM ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EXTREMITY CONTRACTURE ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FOETAL HEART RATE ABNORMAL ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 4 FDA reports)
GRIP STRENGTH DECREASED ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFUSION SITE PRURITUS ( 4 FDA reports)
INTRACRANIAL HAEMATOMA ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LISTLESS ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LOW TURNOVER OSTEOPATHY ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LUNG HERNIA ( 4 FDA reports)
MAMMOGRAM ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
OESOPHAGEAL STENOSIS ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PHARYNGEAL ULCERATION ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
SCAB ( 4 FDA reports)
SCAN ABNORMAL ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 4 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SNORING ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TRAUMATIC FRACTURE ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
WEIGHT BEARING DIFFICULTY ( 4 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ASPLENIA ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
AVERSION ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BONE LOSS ( 3 FDA reports)
BONE METABOLISM DISORDER ( 3 FDA reports)
BOWEN'S DISEASE ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
BUNION ( 3 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONGENITAL HAIR DISORDER ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DEFORMITY THORAX ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DROP ATTACKS ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ECZEMA ASTEATOTIC ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FRACTURE MALUNION ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART INJURY ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HETEROTAXIA ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
ILEUS ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCISION SITE CELLULITIS ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
METASTASES TO MOUTH ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEONATAL TACHYPNOEA ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYP COLORECTAL ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PREMATURE MENOPAUSE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PTERYGIUM COLLI ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
RENAL CANCER ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
SCAN ABDOMEN ABNORMAL ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONGUE ERUPTION ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TURNER'S SYNDROME ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VIRAL CARDIOMYOPATHY ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BIOPSY BONE ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 2 FDA reports)
COMPLICATION OF DELIVERY ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CRANIOSYNOSTOSIS ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GENITAL DISORDER MALE ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HIP DEFORMITY ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL ERYTHEMA ( 2 FDA reports)
LARYNX IRRITATION ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEITIS DEFORMANS ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OXYGEN CONSUMPTION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYURIA ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL ANEURYSM ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SARCOMA OF SKIN ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
TIC ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
UTERINE NEOPLASM ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
YAWNING ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPLICATION SITE COLD FEELING ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER ABLATION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELECTROLYTES ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
CONGENITAL JAW MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL ABRASION ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH OF PET ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE NAEVUS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FISTULA REPAIR ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURED ZYGOMATIC ARCH ELEVATION ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART BLOCK CONGENITAL ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCALCAEMIC NEPHROPATHY ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LARYNGOTRACHEITIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEMIERRE SYNDROME ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL ALLERGY SYNDROME ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OVARIAN FIBROSIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALINDROMIC RHEUMATISM ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL CYST ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERINEAL LACERATION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY OEDEMA NEONATAL ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL TOXICITY ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SITUS INVERSUS ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUBSTANCE ABUSER ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH CROWDING ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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