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

DYSPNOEA ( 491 FDA reports)
DRUG INEFFECTIVE ( 447 FDA reports)
PAIN ( 363 FDA reports)
ANXIETY ( 299 FDA reports)
NAUSEA ( 279 FDA reports)
PNEUMONIA ( 257 FDA reports)
VOMITING ( 208 FDA reports)
ASTHMA ( 207 FDA reports)
COUGH ( 197 FDA reports)
DIZZINESS ( 191 FDA reports)
DIARRHOEA ( 186 FDA reports)
HEADACHE ( 182 FDA reports)
FATIGUE ( 175 FDA reports)
OEDEMA PERIPHERAL ( 171 FDA reports)
DEPRESSION ( 168 FDA reports)
INJURY ( 168 FDA reports)
CHEST PAIN ( 167 FDA reports)
ASTHENIA ( 156 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 151 FDA reports)
CHOLECYSTITIS CHRONIC ( 134 FDA reports)
PULMONARY EMBOLISM ( 134 FDA reports)
ANAEMIA ( 133 FDA reports)
BACK PAIN ( 131 FDA reports)
ABDOMINAL PAIN ( 129 FDA reports)
CHOLELITHIASIS ( 121 FDA reports)
FALL ( 121 FDA reports)
WEIGHT DECREASED ( 120 FDA reports)
PYREXIA ( 119 FDA reports)
ARTHRALGIA ( 116 FDA reports)
DEATH ( 113 FDA reports)
PAIN IN EXTREMITY ( 113 FDA reports)
HYPERTENSION ( 112 FDA reports)
INSOMNIA ( 112 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 109 FDA reports)
DEEP VEIN THROMBOSIS ( 105 FDA reports)
EMOTIONAL DISTRESS ( 102 FDA reports)
PLEURAL EFFUSION ( 101 FDA reports)
CONSTIPATION ( 99 FDA reports)
RENAL FAILURE ( 98 FDA reports)
MUSCLE SPASMS ( 97 FDA reports)
OSTEONECROSIS OF JAW ( 96 FDA reports)
GALLBLADDER DISORDER ( 94 FDA reports)
BRONCHITIS ( 93 FDA reports)
ABDOMINAL PAIN UPPER ( 91 FDA reports)
CEREBROVASCULAR ACCIDENT ( 91 FDA reports)
DECREASED APPETITE ( 91 FDA reports)
DEHYDRATION ( 88 FDA reports)
HYPOAESTHESIA ( 88 FDA reports)
URINARY TRACT INFECTION ( 85 FDA reports)
WHEEZING ( 84 FDA reports)
HYPOKALAEMIA ( 82 FDA reports)
HYPOTENSION ( 80 FDA reports)
MALAISE ( 80 FDA reports)
OSTEOARTHRITIS ( 80 FDA reports)
CHEST DISCOMFORT ( 76 FDA reports)
SYNCOPE ( 75 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 74 FDA reports)
RENAL FAILURE ACUTE ( 74 FDA reports)
CONDITION AGGRAVATED ( 73 FDA reports)
MYALGIA ( 72 FDA reports)
ATRIAL FIBRILLATION ( 71 FDA reports)
MUSCULAR WEAKNESS ( 70 FDA reports)
GAIT DISTURBANCE ( 69 FDA reports)
RASH ( 69 FDA reports)
CONFUSIONAL STATE ( 68 FDA reports)
MYOCARDIAL INFARCTION ( 68 FDA reports)
RESPIRATORY FAILURE ( 68 FDA reports)
SEPSIS ( 66 FDA reports)
TREMOR ( 66 FDA reports)
WEIGHT INCREASED ( 66 FDA reports)
STRESS ( 65 FDA reports)
VISION BLURRED ( 65 FDA reports)
ANHEDONIA ( 63 FDA reports)
BLOOD GLUCOSE INCREASED ( 63 FDA reports)
CONVULSION ( 63 FDA reports)
OSTEOMYELITIS ( 63 FDA reports)
HYPERGLYCAEMIA ( 61 FDA reports)
ATELECTASIS ( 60 FDA reports)
BONE DISORDER ( 60 FDA reports)
DYSPHAGIA ( 60 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 60 FDA reports)
NEUROPATHY PERIPHERAL ( 59 FDA reports)
PAIN IN JAW ( 59 FDA reports)
CELLULITIS ( 58 FDA reports)
PARAESTHESIA ( 58 FDA reports)
PRURITUS ( 58 FDA reports)
HYPERSENSITIVITY ( 55 FDA reports)
LOSS OF CONSCIOUSNESS ( 55 FDA reports)
RENAL IMPAIRMENT ( 55 FDA reports)
SINUSITIS ( 55 FDA reports)
HYPOXIA ( 54 FDA reports)
INFECTION ( 54 FDA reports)
LACTIC ACIDOSIS ( 54 FDA reports)
BLOOD PRESSURE INCREASED ( 53 FDA reports)
CARDIAC ARREST ( 53 FDA reports)
TACHYCARDIA ( 53 FDA reports)
UNEVALUABLE EVENT ( 53 FDA reports)
BALANCE DISORDER ( 52 FDA reports)
FEAR ( 52 FDA reports)
HEART RATE INCREASED ( 50 FDA reports)
SPINAL OSTEOARTHRITIS ( 50 FDA reports)
THROAT IRRITATION ( 50 FDA reports)
CORONARY ARTERY DISEASE ( 49 FDA reports)
ERYTHEMA ( 49 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 48 FDA reports)
THROMBOCYTOPENIA ( 48 FDA reports)
MENTAL DISORDER ( 47 FDA reports)
RECTAL HAEMORRHAGE ( 47 FDA reports)
OROPHARYNGEAL PAIN ( 45 FDA reports)
CARDIOMEGALY ( 44 FDA reports)
CONTUSION ( 44 FDA reports)
HAEMOGLOBIN DECREASED ( 44 FDA reports)
RESPIRATORY DISTRESS ( 44 FDA reports)
NEUTROPENIA ( 43 FDA reports)
SWELLING ( 43 FDA reports)
BLOOD CREATININE INCREASED ( 42 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 42 FDA reports)
MULTI-ORGAN FAILURE ( 42 FDA reports)
AGGRESSION ( 41 FDA reports)
DYSPHONIA ( 41 FDA reports)
EMPHYSEMA ( 41 FDA reports)
MENTAL STATUS CHANGES ( 41 FDA reports)
SWELLING FACE ( 41 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 41 FDA reports)
DYSGEUSIA ( 40 FDA reports)
HALLUCINATION ( 40 FDA reports)
ORAL PAIN ( 40 FDA reports)
PALPITATIONS ( 40 FDA reports)
PANCYTOPENIA ( 40 FDA reports)
RENAL FAILURE CHRONIC ( 40 FDA reports)
SOMNOLENCE ( 40 FDA reports)
VISUAL IMPAIRMENT ( 40 FDA reports)
DRUG INTERACTION ( 39 FDA reports)
FEELING ABNORMAL ( 39 FDA reports)
IMPAIRED HEALING ( 39 FDA reports)
OEDEMA ( 39 FDA reports)
CANDIDIASIS ( 38 FDA reports)
CHILLS ( 38 FDA reports)
PULMONARY OEDEMA ( 38 FDA reports)
RENAL INJURY ( 38 FDA reports)
DYSPEPSIA ( 37 FDA reports)
HYPOGLYCAEMIA ( 37 FDA reports)
MITRAL VALVE INCOMPETENCE ( 37 FDA reports)
NASOPHARYNGITIS ( 37 FDA reports)
PRODUCT QUALITY ISSUE ( 37 FDA reports)
DIABETES MELLITUS ( 36 FDA reports)
HYPERHIDROSIS ( 36 FDA reports)
JOINT SWELLING ( 36 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 36 FDA reports)
VERTIGO ( 36 FDA reports)
ABDOMINAL DISCOMFORT ( 35 FDA reports)
ABDOMINAL DISTENSION ( 35 FDA reports)
DRUG EFFECT DECREASED ( 35 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 35 FDA reports)
SINUS TACHYCARDIA ( 35 FDA reports)
CATARACT ( 34 FDA reports)
LUNG DISORDER ( 34 FDA reports)
MUSCULOSKELETAL PAIN ( 34 FDA reports)
NEOPLASM MALIGNANT ( 34 FDA reports)
OSTEOPOROSIS ( 34 FDA reports)
BRADYCARDIA ( 33 FDA reports)
DENTAL CARIES ( 33 FDA reports)
DRUG HYPERSENSITIVITY ( 33 FDA reports)
OSTEOPENIA ( 33 FDA reports)
SLEEP APNOEA SYNDROME ( 33 FDA reports)
STAPHYLOCOCCAL INFECTION ( 33 FDA reports)
URTICARIA ( 33 FDA reports)
ALOPECIA ( 32 FDA reports)
EXOSTOSIS ( 32 FDA reports)
FLUSHING ( 32 FDA reports)
MOBILITY DECREASED ( 32 FDA reports)
TOOTHACHE ( 32 FDA reports)
BONE LESION ( 31 FDA reports)
CARDIAC DISORDER ( 31 FDA reports)
DECREASED INTEREST ( 31 FDA reports)
DEFORMITY ( 31 FDA reports)
MIGRAINE ( 31 FDA reports)
PRODUCTIVE COUGH ( 31 FDA reports)
NECK PAIN ( 30 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 29 FDA reports)
DRUG DOSE OMISSION ( 29 FDA reports)
METASTASES TO BONE ( 29 FDA reports)
SCAR ( 29 FDA reports)
BONE PAIN ( 28 FDA reports)
CHOLECYSTECTOMY ( 28 FDA reports)
DRY MOUTH ( 28 FDA reports)
DYSPNOEA EXERTIONAL ( 28 FDA reports)
HAEMORRHOIDS ( 28 FDA reports)
HIATUS HERNIA ( 28 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 28 FDA reports)
LUMBAR SPINAL STENOSIS ( 28 FDA reports)
LYMPHADENOPATHY ( 28 FDA reports)
SUICIDE ATTEMPT ( 28 FDA reports)
THROMBOSIS ( 28 FDA reports)
TOOTH DISORDER ( 28 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 28 FDA reports)
VISUAL ACUITY REDUCED ( 28 FDA reports)
BILIARY DYSKINESIA ( 27 FDA reports)
CARDIO-RESPIRATORY ARREST ( 27 FDA reports)
EAR PAIN ( 27 FDA reports)
ECONOMIC PROBLEM ( 27 FDA reports)
OVERDOSE ( 27 FDA reports)
RESPIRATORY DISORDER ( 27 FDA reports)
URINARY INCONTINENCE ( 27 FDA reports)
AMNESIA ( 26 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 26 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 26 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 26 FDA reports)
MEMORY IMPAIRMENT ( 26 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 26 FDA reports)
OFF LABEL USE ( 26 FDA reports)
PLATELET COUNT DECREASED ( 26 FDA reports)
SCOLIOSIS ( 26 FDA reports)
SKIN ULCER ( 26 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 26 FDA reports)
LETHARGY ( 25 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 25 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 25 FDA reports)
OXYGEN SATURATION DECREASED ( 25 FDA reports)
RESTLESS LEGS SYNDROME ( 25 FDA reports)
SUICIDAL IDEATION ( 25 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 25 FDA reports)
ACUTE RESPIRATORY FAILURE ( 24 FDA reports)
CHOLECYSTITIS ( 24 FDA reports)
DIVERTICULUM ( 24 FDA reports)
DYSURIA ( 24 FDA reports)
GASTRITIS ( 24 FDA reports)
GLAUCOMA ( 24 FDA reports)
LEUKOPENIA ( 24 FDA reports)
LUNG NEOPLASM ( 24 FDA reports)
NEPHROLITHIASIS ( 24 FDA reports)
OSTEONECROSIS ( 24 FDA reports)
TINNITUS ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
EXPOSED BONE IN JAW ( 23 FDA reports)
FUNGAL INFECTION ( 23 FDA reports)
GINGIVAL PAIN ( 23 FDA reports)
HIP FRACTURE ( 23 FDA reports)
HYPONATRAEMIA ( 23 FDA reports)
IRRITABLE BOWEL SYNDROME ( 23 FDA reports)
MALNUTRITION ( 23 FDA reports)
PNEUMONITIS ( 23 FDA reports)
STOMATITIS ( 23 FDA reports)
TOOTH ABSCESS ( 23 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 22 FDA reports)
ARRHYTHMIA ( 22 FDA reports)
ARTHROPATHY ( 22 FDA reports)
BURNING SENSATION ( 22 FDA reports)
COLITIS ( 22 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 22 FDA reports)
DISABILITY ( 22 FDA reports)
FISTULA ( 22 FDA reports)
HAEMOPTYSIS ( 22 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 22 FDA reports)
NASAL CONGESTION ( 22 FDA reports)
PANCREATITIS ( 22 FDA reports)
PRIMARY SEQUESTRUM ( 22 FDA reports)
PULMONARY CONGESTION ( 22 FDA reports)
RIB FRACTURE ( 22 FDA reports)
ABNORMAL BEHAVIOUR ( 21 FDA reports)
ARTHRITIS ( 21 FDA reports)
BODY TEMPERATURE INCREASED ( 21 FDA reports)
BRONCHOSPASM ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
CHOLECYSTITIS ACUTE ( 21 FDA reports)
DECUBITUS ULCER ( 21 FDA reports)
HYPOPHAGIA ( 21 FDA reports)
HYPOTHYROIDISM ( 21 FDA reports)
MULTIPLE MYELOMA ( 21 FDA reports)
NERVOUSNESS ( 21 FDA reports)
PNEUMOTHORAX ( 21 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 20 FDA reports)
DRUG DEPENDENCE ( 20 FDA reports)
EPISTAXIS ( 20 FDA reports)
GINGIVAL SWELLING ( 20 FDA reports)
HAEMATEMESIS ( 20 FDA reports)
HAEMATOCHEZIA ( 20 FDA reports)
HEPATIC STEATOSIS ( 20 FDA reports)
HERPES ZOSTER ( 20 FDA reports)
HYPERLIPIDAEMIA ( 20 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 20 FDA reports)
PHARYNGEAL OEDEMA ( 20 FDA reports)
RHEUMATOID ARTHRITIS ( 20 FDA reports)
ROAD TRAFFIC ACCIDENT ( 20 FDA reports)
SKIN DISCOLOURATION ( 20 FDA reports)
AGITATION ( 19 FDA reports)
ANGINA PECTORIS ( 19 FDA reports)
COMPRESSION FRACTURE ( 19 FDA reports)
DRY SKIN ( 19 FDA reports)
FAILURE TO THRIVE ( 19 FDA reports)
GALLBLADDER INJURY ( 19 FDA reports)
HAEMATOCRIT DECREASED ( 19 FDA reports)
HYPERCALCAEMIA ( 19 FDA reports)
INFLUENZA LIKE ILLNESS ( 19 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 19 FDA reports)
MULTIPLE INJURIES ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
PULMONARY HYPERTENSION ( 19 FDA reports)
RETCHING ( 19 FDA reports)
SKIN LESION ( 19 FDA reports)
TREATMENT NONCOMPLIANCE ( 19 FDA reports)
ABASIA ( 18 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 18 FDA reports)
BONE LOSS ( 18 FDA reports)
DYSKINESIA ( 18 FDA reports)
ENCEPHALOPATHY ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
GINGIVITIS ( 18 FDA reports)
HEART RATE IRREGULAR ( 18 FDA reports)
NEUTROPHIL COUNT INCREASED ( 18 FDA reports)
OSTEOLYSIS ( 18 FDA reports)
PNEUMONIA ASPIRATION ( 18 FDA reports)
ABSCESS ( 17 FDA reports)
ANAPHYLACTIC REACTION ( 17 FDA reports)
BLINDNESS ( 17 FDA reports)
BLISTER ( 17 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 17 FDA reports)
CACHEXIA ( 17 FDA reports)
COAGULOPATHY ( 17 FDA reports)
CROHN'S DISEASE ( 17 FDA reports)
DRUG ADMINISTRATION ERROR ( 17 FDA reports)
GANGRENE ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
INFLAMMATION ( 17 FDA reports)
INTENTIONAL OVERDOSE ( 17 FDA reports)
LOCALISED INFECTION ( 17 FDA reports)
LOOSE TOOTH ( 17 FDA reports)
MELAENA ( 17 FDA reports)
RESPIRATORY TRACT INFECTION ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
SPINAL COMPRESSION FRACTURE ( 17 FDA reports)
TYPE 2 DIABETES MELLITUS ( 17 FDA reports)
UNRESPONSIVE TO STIMULI ( 17 FDA reports)
VENTRICULAR TACHYCARDIA ( 17 FDA reports)
AORTIC ANEURYSM ( 16 FDA reports)
ARTERIOSCLEROSIS ( 16 FDA reports)
ATRIAL TACHYCARDIA ( 16 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 16 FDA reports)
CIRCULATORY COLLAPSE ( 16 FDA reports)
CULTURE URINE POSITIVE ( 16 FDA reports)
CYANOSIS ( 16 FDA reports)
DEAFNESS ( 16 FDA reports)
DERMAL CYST ( 16 FDA reports)
DEVICE MALFUNCTION ( 16 FDA reports)
DIPLOPIA ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
FEBRILE NEUTROPENIA ( 16 FDA reports)
LIP SWELLING ( 16 FDA reports)
LUNG INFECTION ( 16 FDA reports)
MEDICATION ERROR ( 16 FDA reports)
NERVOUS SYSTEM DISORDER ( 16 FDA reports)
OBESITY ( 16 FDA reports)
ORAL CANDIDIASIS ( 16 FDA reports)
ORAL DISCOMFORT ( 16 FDA reports)
OSTEOSCLEROSIS ( 16 FDA reports)
SENSORY DISTURBANCE ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
TOOTH INFECTION ( 16 FDA reports)
TOOTH LOSS ( 16 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 15 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 15 FDA reports)
AORTIC VALVE INCOMPETENCE ( 15 FDA reports)
BILIARY COLIC ( 15 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
BLOOD UREA INCREASED ( 15 FDA reports)
COGNITIVE DISORDER ( 15 FDA reports)
COLONIC POLYP ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
ECZEMA ( 15 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 15 FDA reports)
ELECTROLYTE IMBALANCE ( 15 FDA reports)
FLUID RETENTION ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
HEAD INJURY ( 15 FDA reports)
HYPERKALAEMIA ( 15 FDA reports)
INFLUENZA ( 15 FDA reports)
INJECTION SITE PAIN ( 15 FDA reports)
IRRITABILITY ( 15 FDA reports)
LEUKOCYTOSIS ( 15 FDA reports)
LUNG NEOPLASM MALIGNANT ( 15 FDA reports)
MOOD SWINGS ( 15 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 15 FDA reports)
PERIODONTITIS ( 15 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 15 FDA reports)
SPINAL COLUMN STENOSIS ( 15 FDA reports)
SPINAL CORD COMPRESSION ( 15 FDA reports)
TENDERNESS ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
VIRAL INFECTION ( 15 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 14 FDA reports)
BLOOD GLUCOSE DECREASED ( 14 FDA reports)
CHOLESTEROSIS ( 14 FDA reports)
DIVERTICULITIS ( 14 FDA reports)
ERECTILE DYSFUNCTION ( 14 FDA reports)
FEELING COLD ( 14 FDA reports)
HAEMATOMA ( 14 FDA reports)
MACULAR DEGENERATION ( 14 FDA reports)
MASTICATION DISORDER ( 14 FDA reports)
MOUTH ULCERATION ( 14 FDA reports)
OESOPHAGITIS ( 14 FDA reports)
PANIC ATTACK ( 14 FDA reports)
POLLAKIURIA ( 14 FDA reports)
PRESYNCOPE ( 14 FDA reports)
PSYCHOTIC DISORDER ( 14 FDA reports)
RENAL CYST ( 14 FDA reports)
RENAL DISORDER ( 14 FDA reports)
RESTLESSNESS ( 14 FDA reports)
RHINITIS ( 14 FDA reports)
SINUS CONGESTION ( 14 FDA reports)
SLEEP DISORDER ( 14 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 13 FDA reports)
AGEUSIA ( 13 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
BLOOD CALCIUM DECREASED ( 13 FDA reports)
BRONCHIECTASIS ( 13 FDA reports)
COLITIS ULCERATIVE ( 13 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
DRY EYE ( 13 FDA reports)
ESCHERICHIA INFECTION ( 13 FDA reports)
EXPIRED DRUG ADMINISTERED ( 13 FDA reports)
GRAND MAL CONVULSION ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
HEPATIC ENZYME INCREASED ( 13 FDA reports)
HOSPITALISATION ( 13 FDA reports)
INCORRECT DOSE ADMINISTERED ( 13 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 13 FDA reports)
MUCOSAL INFLAMMATION ( 13 FDA reports)
OCULAR HYPERAEMIA ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
ROTATOR CUFF SYNDROME ( 13 FDA reports)
SKIN DISORDER ( 13 FDA reports)
SKIN INDURATION ( 13 FDA reports)
ACTINOMYCOSIS ( 12 FDA reports)
ATAXIA ( 12 FDA reports)
BASAL CELL CARCINOMA ( 12 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 12 FDA reports)
BURSITIS ( 12 FDA reports)
CARDIAC MURMUR ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
CHOKING ( 12 FDA reports)
CYSTITIS ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
DYSLIPIDAEMIA ( 12 FDA reports)
DYSSTASIA ( 12 FDA reports)
EJECTION FRACTION DECREASED ( 12 FDA reports)
EPIDURAL LIPOMATOSIS ( 12 FDA reports)
GENERALISED OEDEMA ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
HOT FLUSH ( 12 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 12 FDA reports)
INGUINAL HERNIA ( 12 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 12 FDA reports)
LUNG INFILTRATION ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
PHARYNGITIS ( 12 FDA reports)
PLEURITIC PAIN ( 12 FDA reports)
PULMONARY FIBROSIS ( 12 FDA reports)
SINUS DISORDER ( 12 FDA reports)
SKIN HYPERTROPHY ( 12 FDA reports)
STRESS FRACTURE ( 12 FDA reports)
SWOLLEN TONGUE ( 12 FDA reports)
THYROID NEOPLASM ( 12 FDA reports)
URINARY RETENTION ( 12 FDA reports)
WOUND DEHISCENCE ( 12 FDA reports)
ASCITES ( 11 FDA reports)
ASPIRATION ( 11 FDA reports)
BLINDNESS UNILATERAL ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 11 FDA reports)
BRONCHOPNEUMONIA ( 11 FDA reports)
CEREBRAL ATROPHY ( 11 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 11 FDA reports)
CUSHINGOID ( 11 FDA reports)
DIVERTICULUM INTESTINAL ( 11 FDA reports)
EATING DISORDER ( 11 FDA reports)
EMOTIONAL DISORDER ( 11 FDA reports)
FACIAL BONES FRACTURE ( 11 FDA reports)
FEELING JITTERY ( 11 FDA reports)
GASTRIC DISORDER ( 11 FDA reports)
HEARING IMPAIRED ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
HYPERCHOLESTEROLAEMIA ( 11 FDA reports)
HYPOAESTHESIA ORAL ( 11 FDA reports)
ILL-DEFINED DISORDER ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
OSTEITIS ( 11 FDA reports)
OVARIAN CYST ( 11 FDA reports)
OXYGEN SATURATION ABNORMAL ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
PERIODONTAL DISEASE ( 11 FDA reports)
PLEURAL FIBROSIS ( 11 FDA reports)
PROCEDURAL PAIN ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
RHINORRHOEA ( 11 FDA reports)
SCAB ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 11 FDA reports)
THROAT TIGHTNESS ( 11 FDA reports)
WALKING AID USER ( 11 FDA reports)
ABORTION SPONTANEOUS ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
ASTIGMATISM ( 10 FDA reports)
AZOTAEMIA ( 10 FDA reports)
BONE NEOPLASM MALIGNANT ( 10 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 10 FDA reports)
CARDIOMYOPATHY ( 10 FDA reports)
COLITIS ISCHAEMIC ( 10 FDA reports)
DEPRESSED MOOD ( 10 FDA reports)
DEVICE FAILURE ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
EMPYEMA ( 10 FDA reports)
FLANK PAIN ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 10 FDA reports)
GASTRIC ULCER ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
GINGIVAL INFECTION ( 10 FDA reports)
GOITRE ( 10 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 10 FDA reports)
HICCUPS ( 10 FDA reports)
HYPERREFLEXIA ( 10 FDA reports)
HYPOKINESIA ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
KLEBSIELLA INFECTION ( 10 FDA reports)
LIGAMENT SPRAIN ( 10 FDA reports)
LIMB DISCOMFORT ( 10 FDA reports)
LOBAR PNEUMONIA ( 10 FDA reports)
MEDICAL DEVICE COMPLICATION ( 10 FDA reports)
MENORRHAGIA ( 10 FDA reports)
MENTAL IMPAIRMENT ( 10 FDA reports)
MYOCLONUS ( 10 FDA reports)
NEOPLASM PROGRESSION ( 10 FDA reports)
PERICARDIAL EFFUSION ( 10 FDA reports)
PROTHROMBIN TIME PROLONGED ( 10 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 10 FDA reports)
SALIVARY HYPERSECRETION ( 10 FDA reports)
SEBORRHOEIC DERMATITIS ( 10 FDA reports)
SINUS BRADYCARDIA ( 10 FDA reports)
SKIN FIBROSIS ( 10 FDA reports)
SKIN TIGHTNESS ( 10 FDA reports)
SURGERY ( 10 FDA reports)
ULCER ( 10 FDA reports)
ABDOMINAL HERNIA ( 9 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 9 FDA reports)
BACTERIAL INFECTION ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BRONCHIOLITIS ( 9 FDA reports)
CATARACT OPERATION ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
CHANGE OF BOWEL HABIT ( 9 FDA reports)
CLONUS ( 9 FDA reports)
COMA ( 9 FDA reports)
DEMENTIA ( 9 FDA reports)
DENTAL PROSTHESIS USER ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
ENTEROCOCCAL INFECTION ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
FAMILY STRESS ( 9 FDA reports)
FOOT FRACTURE ( 9 FDA reports)
GLOSSODYNIA ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERMETROPIA ( 9 FDA reports)
HYPOACUSIS ( 9 FDA reports)
HYPOAESTHESIA FACIAL ( 9 FDA reports)
HYPOCALCAEMIA ( 9 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 9 FDA reports)
JOINT INJURY ( 9 FDA reports)
LARYNGITIS ( 9 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 9 FDA reports)
MENSTRUATION IRREGULAR ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 9 FDA reports)
MYOSITIS ( 9 FDA reports)
NOCTURIA ( 9 FDA reports)
NODULE ( 9 FDA reports)
ODYNOPHAGIA ( 9 FDA reports)
ORAL DISORDER ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
PLANTAR FASCIITIS ( 9 FDA reports)
PLEURISY ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SENSITIVITY OF TEETH ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SOCIAL PROBLEM ( 9 FDA reports)
SYNOVIAL CYST ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
VAGINAL HAEMORRHAGE ( 9 FDA reports)
X-RAY ABNORMAL ( 9 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 8 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
ANXIETY DISORDER ( 8 FDA reports)
AORTIC DISORDER ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 8 FDA reports)
BLEPHARITIS ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
BRUXISM ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
CLOSTRIDIAL INFECTION ( 8 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
COORDINATION ABNORMAL ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DEVICE RELATED INFECTION ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
EYE SWELLING ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
FIBROMYALGIA ( 8 FDA reports)
FIBROSIS ( 8 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
GINGIVAL RECESSION ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
HYPERTONIA ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
INCREASED BRONCHIAL SECRETION ( 8 FDA reports)
INJECTION SITE HAEMATOMA ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
JOINT DISLOCATION ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LIFE EXPECTANCY SHORTENED ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
MACULAR HOLE ( 8 FDA reports)
MENISCUS LESION ( 8 FDA reports)
METASTASES TO LYMPH NODES ( 8 FDA reports)
MUSCLE TIGHTNESS ( 8 FDA reports)
MUSCLE TWITCHING ( 8 FDA reports)
NASAL SEPTUM DEVIATION ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
PERIPHERAL COLDNESS ( 8 FDA reports)
PERONEAL NERVE PALSY ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
PULMONARY INFARCTION ( 8 FDA reports)
PURULENT DISCHARGE ( 8 FDA reports)
RALES ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 8 FDA reports)
RESPIRATORY RATE INCREASED ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
THIRST ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VENOUS INSUFFICIENCY ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ABDOMINAL TENDERNESS ( 7 FDA reports)
ABSCESS DRAINAGE ( 7 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
AORTIC STENOSIS ( 7 FDA reports)
APHASIA ( 7 FDA reports)
APHONIA ( 7 FDA reports)
ATRIAL SEPTAL DEFECT ( 7 FDA reports)
ATROPHIC VULVOVAGINITIS ( 7 FDA reports)
BACK DISORDER ( 7 FDA reports)
BREAST CANCER RECURRENT ( 7 FDA reports)
BREATH ODOUR ( 7 FDA reports)
CAROTID ARTERY STENOSIS ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CRYING ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DEVICE OCCLUSION ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
DIASTOLIC DYSFUNCTION ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
DYSPHEMIA ( 7 FDA reports)
DYSPLASTIC NAEVUS ( 7 FDA reports)
ESSENTIAL HYPERTENSION ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
HAND FRACTURE ( 7 FDA reports)
HEPATIC ENZYME ABNORMAL ( 7 FDA reports)
HYPERTHYROIDISM ( 7 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INTENTIONAL DRUG MISUSE ( 7 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
METASTASIS ( 7 FDA reports)
MIDDLE INSOMNIA ( 7 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 7 FDA reports)
MYELOMA RECURRENCE ( 7 FDA reports)
NECK MASS ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RETINOPATHY ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SCHIZOPHRENIA ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
TALIPES ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
TOOTH EXTRACTION ( 7 FDA reports)
TOOTH INJURY ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
VAGINAL INFECTION ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 7 FDA reports)
VITAMIN B12 DEFICIENCY ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABSCESS JAW ( 6 FDA reports)
ACROCHORDON ( 6 FDA reports)
ACTINIC ELASTOSIS ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 6 FDA reports)
ANGER ( 6 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
BLOOD IRON DECREASED ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CERVICAL MYELOPATHY ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DENTURE WEARER ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
GALLBLADDER POLYP ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LUMBAR RADICULOPATHY ( 6 FDA reports)
LUNG CONSOLIDATION ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MELANOCYTIC NAEVUS ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PAPULE ( 6 FDA reports)
PARAPLEGIA ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
PLASMACYTOSIS ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 6 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 6 FDA reports)
PULPITIS DENTAL ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RIGHT VENTRICULAR FAILURE ( 6 FDA reports)
SINUS HEADACHE ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
STATUS ASTHMATICUS ( 6 FDA reports)
TOOTH FRACTURE ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
UTERINE LEIOMYOMA ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 5 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 5 FDA reports)
ANEURYSM ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC DILATATION ( 5 FDA reports)
AORTIC VALVE STENOSIS ( 5 FDA reports)
APNOEA ( 5 FDA reports)
ASTHMATIC CRISIS ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CERVICAL DYSPLASIA ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHOROIDAL DETACHMENT ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CONGENITAL ANOMALY ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
CORONARY ARTERY BYPASS ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
CYST ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 5 FDA reports)
DEVICE MISUSE ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DROP ATTACKS ( 5 FDA reports)
DYSAESTHESIA ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
EDENTULOUS ( 5 FDA reports)
EJECTION FRACTION ABNORMAL ( 5 FDA reports)
ENDOMETRIOSIS ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
GOUT ( 5 FDA reports)
HAEMANGIOMA ( 5 FDA reports)
HAEMATOCRIT ABNORMAL ( 5 FDA reports)
HAEMATOCRIT INCREASED ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEARING AID USER ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HILAR LYMPHADENOPATHY ( 5 FDA reports)
HUMERUS FRACTURE ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
ISCHAEMIC HEPATITIS ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
KIDNEY SMALL ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
MANIA ( 5 FDA reports)
MASS ( 5 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
METATARSALGIA ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
MORTON'S NEUROMA ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MULTIPLE FRACTURES ( 5 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
OPTIC NERVE CUPPING ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
ORAL INFECTION ( 5 FDA reports)
OROPHARYNGEAL SPASM ( 5 FDA reports)
OSTEITIS DEFORMANS ( 5 FDA reports)
OSTEOMA ( 5 FDA reports)
PAROSMIA ( 5 FDA reports)
PATHOLOGICAL FRACTURE ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PLASMACYTOMA ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POLYDIPSIA ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PRESBYOPIA ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PULMONARY GRANULOMA ( 5 FDA reports)
PULMONARY RADIATION INJURY ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 5 FDA reports)
RADICULITIS LUMBOSACRAL ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
SALIVARY GLAND MASS ( 5 FDA reports)
SEDATION ( 5 FDA reports)
SOFT TISSUE INFLAMMATION ( 5 FDA reports)
SPINAL FRACTURE ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
TRYPTASE INCREASED ( 5 FDA reports)
UMBILICAL HERNIA ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VIITH NERVE PARALYSIS ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
VOMITING PROJECTILE ( 5 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
ADRENAL SUPPRESSION ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ASTEATOSIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BLADDER NECK OPERATION ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
BONE FISSURE ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CHRONIC SINUSITIS ( 4 FDA reports)
COLPOCELE ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CORNEAL OPERATION ( 4 FDA reports)
CYSTITIS INTERSTITIAL ( 4 FDA reports)
CYSTOPEXY ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DENTAL NECROSIS ( 4 FDA reports)
DEVELOPMENTAL DELAY ( 4 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE NAEVUS ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GASTRODUODENITIS ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
GRIP STRENGTH DECREASED ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HEART VALVE CALCIFICATION ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
IMPAIRED FASTING GLUCOSE ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE PALLOR ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
IRITIS ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MELANOMA RECURRENT ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
OLIGODIPSIA ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ORAL DISCHARGE ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
ORAL PRURITUS ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OSTEOCHONDROSIS ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PARATHYROIDECTOMY ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROSTATIC OBSTRUCTION ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY VALVE STENOSIS ( 4 FDA reports)
RADIOTHERAPY ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
SALIVARY GLAND PAIN ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
SNORING ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 4 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
VAGINAL PROLAPSE ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VASCULAR CALCIFICATION ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VESICAL FISTULA ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
ADNEXA UTERI CYST ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE FRAGMENTATION ( 3 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST NEOPLASM ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BRONCHOSPASM PARADOXICAL ( 3 FDA reports)
CALCIFICATION METASTATIC ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 3 FDA reports)
CONJUNCTIVAL ABRASION ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CONJUNCTIVITIS VIRAL ( 3 FDA reports)
COR PULMONALE CHRONIC ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
CYSTOSCOPY ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACET JOINT SYNDROME ( 3 FDA reports)
FACIAL NEURALGIA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FAECALURIA ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GINGIVAL EROSION ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INHALATION THERAPY ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
JOINT ARTHROPLASTY ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
LEUKODYSTROPHY ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
MACULAR SCAR ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MALOCCLUSION ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
METASTATIC PAIN ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 3 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MOUTH CYST ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESOPHAGEAL POLYP ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OVARIAN CYST RUPTURED ( 3 FDA reports)
PALATAL DISORDER ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYP ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PROCTOCOLITIS ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PYOGENIC GRANULOMA ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RECTAL POLYP ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
THORACIC OUTLET SYNDROME ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONGUE NEOPLASM ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRAUMATIC RENAL INJURY ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 3 FDA reports)
URETHRAL CARUNCLE ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
UTERINE ENLARGEMENT ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
VITREOUS DEGENERATION ( 3 FDA reports)
VITREOUS DETACHMENT ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIAL SPASM ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ASTROCYTOMA ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIAL DIARRHOEA ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALUMINIUM INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BONE SCAN ABNORMAL ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONGENITAL CYSTIC LUNG ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DISORDER OF ORBIT ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EXPOSURE TO MOULD ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL OEDEMA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERNIA OBSTRUCTIVE ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPLANT SITE EXTRAVASATION ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INFECTIVE TENOSYNOVITIS ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INGUINAL HERNIA STRANGULATED ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 2 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
INTRAOSSEOUS ANGIOMA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACROPHAGES INCREASED ( 2 FDA reports)
MASTOCYTOSIS ( 2 FDA reports)
MECONIUM STAIN ( 2 FDA reports)
MEDICAL DEVICE CHANGE ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MILK-ALKALI SYNDROME ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROANTRAL FISTULA ( 2 FDA reports)
OROPHARYNGITIS FUNGAL ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTMENOPAUSE ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SERONEGATIVE ARTHRITIS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPERMATOZOA ABNORMAL ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBMANDIBULAR MASS ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SYDENHAM'S CHOREA ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULAR MALFORMATION PERIPHERAL ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL TEST NEGATIVE ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH ALCOHOL TEST NEGATIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVICAL NEURITIS ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CNS GERMINOMA ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL TERATOMA ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTIC FIBROSIS RELATED DIABETES ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DEVICE THERAPY ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDIAL FIBROELASTOSIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROPARESIS POSTOPERATIVE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEAL GANGRENE ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 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)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED ANTEROPOSTERIOR CHEST DIAMETER ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERLEUKIN LEVEL DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATITIS INTERSTITIAL ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO MOUTH ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MIXED OLIGO-ASTROCYTOMA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYELOMALACIA ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OMENTUM NEOPLASM ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOMYELITIS DRAINAGE ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCOAST'S TUMOUR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PERICHONDRITIS ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYCYSTIC LIVER DISEASE ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHINITIS PERENNIAL ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPUTUM DECREASED ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STARING ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE ANALYSIS ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URTICARIA AQUAGENIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
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UTERINE POLYP ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VASOPRESSIN CHALLENGE TEST ABNORMAL ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
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VERBAL ABUSE ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
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VIRAL CARDIOMYOPATHY ( 1 FDA reports)
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VITAMIN B12 DECREASED ( 1 FDA reports)
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WALKING DISABILITY ( 1 FDA reports)
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WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)

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