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

DYSPNOEA ( 1167 FDA reports)
PNEUMONIA ( 772 FDA reports)
PAIN ( 649 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 636 FDA reports)
NAUSEA ( 597 FDA reports)
ASTHMA ( 558 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 541 FDA reports)
ASTHENIA ( 514 FDA reports)
DEATH ( 491 FDA reports)
ANXIETY ( 489 FDA reports)
VOMITING ( 466 FDA reports)
DRUG INEFFECTIVE ( 463 FDA reports)
FATIGUE ( 459 FDA reports)
DIZZINESS ( 450 FDA reports)
OEDEMA PERIPHERAL ( 442 FDA reports)
ATRIAL FIBRILLATION ( 434 FDA reports)
DIARRHOEA ( 433 FDA reports)
ANAEMIA ( 427 FDA reports)
HEADACHE ( 422 FDA reports)
CHEST PAIN ( 398 FDA reports)
HYPOTENSION ( 396 FDA reports)
PYREXIA ( 392 FDA reports)
RESPIRATORY FAILURE ( 392 FDA reports)
HYPERTENSION ( 390 FDA reports)
COUGH ( 367 FDA reports)
FALL ( 359 FDA reports)
WEIGHT DECREASED ( 358 FDA reports)
INJURY ( 345 FDA reports)
DEPRESSION ( 339 FDA reports)
MYOCARDIAL INFARCTION ( 338 FDA reports)
CONDITION AGGRAVATED ( 323 FDA reports)
ARTHRALGIA ( 297 FDA reports)
RENAL FAILURE ACUTE ( 295 FDA reports)
CONSTIPATION ( 290 FDA reports)
CONFUSIONAL STATE ( 288 FDA reports)
MALAISE ( 282 FDA reports)
BRONCHITIS ( 279 FDA reports)
RENAL FAILURE ( 279 FDA reports)
BACK PAIN ( 273 FDA reports)
PAIN IN EXTREMITY ( 273 FDA reports)
PLEURAL EFFUSION ( 266 FDA reports)
SEPSIS ( 261 FDA reports)
URINARY TRACT INFECTION ( 260 FDA reports)
ABDOMINAL PAIN ( 246 FDA reports)
DEHYDRATION ( 234 FDA reports)
PULMONARY EMBOLISM ( 225 FDA reports)
CORONARY ARTERY DISEASE ( 219 FDA reports)
SINUSITIS ( 217 FDA reports)
CEREBROVASCULAR ACCIDENT ( 212 FDA reports)
WHEEZING ( 210 FDA reports)
RASH ( 209 FDA reports)
CARDIAC ARREST ( 201 FDA reports)
CHEST DISCOMFORT ( 199 FDA reports)
TREMOR ( 196 FDA reports)
ECONOMIC PROBLEM ( 195 FDA reports)
TACHYCARDIA ( 194 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 193 FDA reports)
OSTEOARTHRITIS ( 191 FDA reports)
DECREASED APPETITE ( 185 FDA reports)
MUSCLE SPASMS ( 180 FDA reports)
MITRAL VALVE INCOMPETENCE ( 179 FDA reports)
PRURITUS ( 178 FDA reports)
THROMBOCYTOPENIA ( 178 FDA reports)
INSOMNIA ( 177 FDA reports)
DYSPHAGIA ( 173 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 173 FDA reports)
CARDIOMEGALY ( 170 FDA reports)
ATELECTASIS ( 169 FDA reports)
CARDIO-RESPIRATORY ARREST ( 169 FDA reports)
HAEMOGLOBIN DECREASED ( 168 FDA reports)
HYPOAESTHESIA ( 168 FDA reports)
RESPIRATORY DISTRESS ( 167 FDA reports)
BLOOD PRESSURE INCREASED ( 166 FDA reports)
DIABETES MELLITUS ( 165 FDA reports)
SYNCOPE ( 165 FDA reports)
CONVULSION ( 163 FDA reports)
HEART RATE INCREASED ( 161 FDA reports)
HYPERHIDROSIS ( 161 FDA reports)
VISION BLURRED ( 160 FDA reports)
NEUROPATHY PERIPHERAL ( 159 FDA reports)
MYALGIA ( 157 FDA reports)
PULMONARY OEDEMA ( 157 FDA reports)
DRUG INTERACTION ( 156 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 154 FDA reports)
SOMNOLENCE ( 154 FDA reports)
BLOOD GLUCOSE INCREASED ( 149 FDA reports)
CELLULITIS ( 145 FDA reports)
EMPHYSEMA ( 145 FDA reports)
OSTEONECROSIS OF JAW ( 145 FDA reports)
FEELING ABNORMAL ( 142 FDA reports)
PULMONARY HYPERTENSION ( 142 FDA reports)
INFECTION ( 141 FDA reports)
BRADYCARDIA ( 140 FDA reports)
HYPERSENSITIVITY ( 140 FDA reports)
CATARACT ( 139 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 138 FDA reports)
GAIT DISTURBANCE ( 136 FDA reports)
HAEMOPTYSIS ( 136 FDA reports)
OSTEOMYELITIS ( 133 FDA reports)
CHILLS ( 132 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 132 FDA reports)
HYPOKALAEMIA ( 132 FDA reports)
CONTUSION ( 131 FDA reports)
EMOTIONAL DISTRESS ( 131 FDA reports)
HYPOXIA ( 131 FDA reports)
RENAL FAILURE CHRONIC ( 131 FDA reports)
DEEP VEIN THROMBOSIS ( 130 FDA reports)
DYSPEPSIA ( 129 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 129 FDA reports)
PARAESTHESIA ( 129 FDA reports)
WEIGHT INCREASED ( 129 FDA reports)
ANHEDONIA ( 128 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 128 FDA reports)
ABDOMINAL PAIN UPPER ( 126 FDA reports)
PALPITATIONS ( 126 FDA reports)
LOSS OF CONSCIOUSNESS ( 125 FDA reports)
BLOOD CREATININE INCREASED ( 123 FDA reports)
MULTI-ORGAN FAILURE ( 122 FDA reports)
DYSPHONIA ( 121 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 119 FDA reports)
HYPONATRAEMIA ( 119 FDA reports)
NECK PAIN ( 119 FDA reports)
MULTIPLE INJURIES ( 118 FDA reports)
BONE DISORDER ( 117 FDA reports)
VENTRICULAR TACHYCARDIA ( 117 FDA reports)
CARDIAC FAILURE ( 116 FDA reports)
MEMORY IMPAIRMENT ( 116 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 116 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 116 FDA reports)
MUSCULAR WEAKNESS ( 115 FDA reports)
NASOPHARYNGITIS ( 114 FDA reports)
CARDIAC DISORDER ( 113 FDA reports)
DYSPNOEA EXERTIONAL ( 113 FDA reports)
OSTEOPOROSIS ( 112 FDA reports)
SEPTIC SHOCK ( 111 FDA reports)
SPINAL OSTEOARTHRITIS ( 110 FDA reports)
ANGINA PECTORIS ( 109 FDA reports)
BONE PAIN ( 109 FDA reports)
MENTAL STATUS CHANGES ( 109 FDA reports)
PAIN IN JAW ( 109 FDA reports)
PANCYTOPENIA ( 109 FDA reports)
ACUTE RESPIRATORY FAILURE ( 106 FDA reports)
GASTRITIS ( 105 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 104 FDA reports)
OEDEMA ( 104 FDA reports)
HYPERKALAEMIA ( 103 FDA reports)
OSTEONECROSIS ( 103 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 102 FDA reports)
HYPERGLYCAEMIA ( 102 FDA reports)
RECTAL HAEMORRHAGE ( 102 FDA reports)
ERYTHEMA ( 101 FDA reports)
OVERDOSE ( 100 FDA reports)
URTICARIA ( 100 FDA reports)
EJECTION FRACTION DECREASED ( 99 FDA reports)
LETHARGY ( 99 FDA reports)
SURGERY ( 99 FDA reports)
SWELLING ( 99 FDA reports)
UNEVALUABLE EVENT ( 99 FDA reports)
HYPERLIPIDAEMIA ( 98 FDA reports)
COMA ( 97 FDA reports)
LUNG DISORDER ( 97 FDA reports)
PRODUCTIVE COUGH ( 97 FDA reports)
BLOOD PRESSURE DECREASED ( 96 FDA reports)
EPISTAXIS ( 95 FDA reports)
OXYGEN SATURATION DECREASED ( 95 FDA reports)
CHOLELITHIASIS ( 93 FDA reports)
DIVERTICULUM ( 93 FDA reports)
HAEMORRHAGE ( 92 FDA reports)
ABDOMINAL DISTENSION ( 91 FDA reports)
COAGULOPATHY ( 91 FDA reports)
LUNG INFILTRATION ( 91 FDA reports)
HAEMATOCRIT DECREASED ( 90 FDA reports)
RIB FRACTURE ( 89 FDA reports)
BRONCHOSPASM ( 87 FDA reports)
CYANOSIS ( 87 FDA reports)
DISORIENTATION ( 87 FDA reports)
TOOTH EXTRACTION ( 87 FDA reports)
DENTAL CARIES ( 86 FDA reports)
ARTERIOSCLEROSIS ( 85 FDA reports)
SINUS TACHYCARDIA ( 85 FDA reports)
ARTHRITIS ( 84 FDA reports)
BALANCE DISORDER ( 84 FDA reports)
SLEEP APNOEA SYNDROME ( 83 FDA reports)
TREATMENT NONCOMPLIANCE ( 82 FDA reports)
MOBILITY DECREASED ( 81 FDA reports)
SPINAL COMPRESSION FRACTURE ( 81 FDA reports)
URINARY RETENTION ( 81 FDA reports)
ARRHYTHMIA ( 80 FDA reports)
HIATUS HERNIA ( 80 FDA reports)
UNRESPONSIVE TO STIMULI ( 80 FDA reports)
PLATELET COUNT DECREASED ( 79 FDA reports)
AGITATION ( 78 FDA reports)
INTERSTITIAL LUNG DISEASE ( 78 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 78 FDA reports)
DRY MOUTH ( 76 FDA reports)
RENAL IMPAIRMENT ( 76 FDA reports)
SPINAL COLUMN STENOSIS ( 76 FDA reports)
STAPHYLOCOCCAL INFECTION ( 76 FDA reports)
HYPOGLYCAEMIA ( 75 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 75 FDA reports)
HAEMATURIA ( 74 FDA reports)
NERVOUSNESS ( 74 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 73 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 73 FDA reports)
CANDIDIASIS ( 72 FDA reports)
HEART RATE IRREGULAR ( 72 FDA reports)
HEPATIC FAILURE ( 72 FDA reports)
LYMPHADENOPATHY ( 72 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 72 FDA reports)
POLLAKIURIA ( 72 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 71 FDA reports)
CARDIOMYOPATHY ( 71 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 71 FDA reports)
LUNG NEOPLASM ( 71 FDA reports)
MENTAL DISORDER ( 71 FDA reports)
METASTASES TO BONE ( 71 FDA reports)
MYOCARDIAL ISCHAEMIA ( 71 FDA reports)
AMNESIA ( 70 FDA reports)
BLOOD UREA INCREASED ( 70 FDA reports)
HERPES ZOSTER ( 70 FDA reports)
SWELLING FACE ( 69 FDA reports)
THROMBOSIS ( 69 FDA reports)
DISEASE PROGRESSION ( 68 FDA reports)
RESPIRATORY ARREST ( 68 FDA reports)
STRESS ( 68 FDA reports)
JOINT SWELLING ( 67 FDA reports)
PRODUCT QUALITY ISSUE ( 67 FDA reports)
RHINORRHOEA ( 67 FDA reports)
ABASIA ( 66 FDA reports)
BURSITIS ( 66 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 66 FDA reports)
LEUKOCYTOSIS ( 66 FDA reports)
MIGRAINE ( 66 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 65 FDA reports)
IMPAIRED HEALING ( 65 FDA reports)
MEDICATION ERROR ( 65 FDA reports)
RESPIRATORY TRACT INFECTION ( 65 FDA reports)
URINARY INCONTINENCE ( 65 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 64 FDA reports)
DRUG HYPERSENSITIVITY ( 64 FDA reports)
HYPERCHOLESTEROLAEMIA ( 64 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 64 FDA reports)
TACHYPNOEA ( 64 FDA reports)
TYPE 2 DIABETES MELLITUS ( 64 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 63 FDA reports)
MALNUTRITION ( 63 FDA reports)
NASAL CONGESTION ( 63 FDA reports)
ROTATOR CUFF SYNDROME ( 63 FDA reports)
ABSCESS ( 62 FDA reports)
ANOREXIA ( 62 FDA reports)
COLONIC POLYP ( 62 FDA reports)
DIPLOPIA ( 62 FDA reports)
FEAR ( 62 FDA reports)
HALLUCINATION ( 62 FDA reports)
ILL-DEFINED DISORDER ( 62 FDA reports)
MUSCULOSKELETAL PAIN ( 62 FDA reports)
ORAL CANDIDIASIS ( 62 FDA reports)
OSTEOPENIA ( 62 FDA reports)
CAROTID ARTERY STENOSIS ( 61 FDA reports)
DRUG DEPENDENCE ( 61 FDA reports)
SPEECH DISORDER ( 61 FDA reports)
VERTIGO ( 61 FDA reports)
ALOPECIA ( 60 FDA reports)
ARTHROPATHY ( 60 FDA reports)
BLISTER ( 60 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 60 FDA reports)
CARDIOVASCULAR DISORDER ( 60 FDA reports)
DYSGEUSIA ( 60 FDA reports)
ENCEPHALOPATHY ( 60 FDA reports)
HYPOTHYROIDISM ( 60 FDA reports)
LUNG NEOPLASM MALIGNANT ( 60 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 60 FDA reports)
MULTIPLE MYELOMA ( 60 FDA reports)
NEUTROPENIA ( 60 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 60 FDA reports)
SKIN EXFOLIATION ( 60 FDA reports)
SLEEP DISORDER ( 60 FDA reports)
BURNING SENSATION ( 59 FDA reports)
CEREBRAL ATROPHY ( 59 FDA reports)
PULMONARY CONGESTION ( 59 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 58 FDA reports)
BLOOD BILIRUBIN INCREASED ( 58 FDA reports)
DYSURIA ( 58 FDA reports)
HAEMATOMA ( 58 FDA reports)
LUNG INFECTION ( 58 FDA reports)
NEOPLASM MALIGNANT ( 58 FDA reports)
APNOEA ( 57 FDA reports)
MASS ( 57 FDA reports)
MELAENA ( 57 FDA reports)
RALES ( 57 FDA reports)
SPUTUM DISCOLOURED ( 57 FDA reports)
SUICIDAL IDEATION ( 57 FDA reports)
ABDOMINAL DISCOMFORT ( 56 FDA reports)
AORTIC VALVE INCOMPETENCE ( 56 FDA reports)
BRONCHOPNEUMONIA ( 56 FDA reports)
PERICARDIAL EFFUSION ( 56 FDA reports)
PROTHROMBIN TIME PROLONGED ( 56 FDA reports)
VENTRICULAR HYPERTROPHY ( 56 FDA reports)
VISUAL IMPAIRMENT ( 56 FDA reports)
BLOOD ALBUMIN DECREASED ( 55 FDA reports)
FLUID RETENTION ( 55 FDA reports)
ASCITES ( 54 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 54 FDA reports)
INFLUENZA ( 54 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 54 FDA reports)
THROAT IRRITATION ( 54 FDA reports)
DECREASED INTEREST ( 53 FDA reports)
HAEMORRHOIDS ( 53 FDA reports)
LEFT ATRIAL DILATATION ( 53 FDA reports)
OBESITY ( 53 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 52 FDA reports)
CARDIAC MURMUR ( 52 FDA reports)
ATRIAL FLUTTER ( 51 FDA reports)
DISABILITY ( 51 FDA reports)
MASTICATION DISORDER ( 51 FDA reports)
ORAL PAIN ( 51 FDA reports)
ORTHOSTATIC HYPOTENSION ( 51 FDA reports)
RESPIRATORY RATE INCREASED ( 51 FDA reports)
ROAD TRAFFIC ACCIDENT ( 50 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 50 FDA reports)
ACUTE PULMONARY OEDEMA ( 49 FDA reports)
EMOTIONAL DISORDER ( 49 FDA reports)
GASTRIC ULCER ( 49 FDA reports)
HEMIPARESIS ( 49 FDA reports)
INCORRECT DOSE ADMINISTERED ( 49 FDA reports)
TINNITUS ( 49 FDA reports)
TOOTH DISORDER ( 49 FDA reports)
BLOOD SODIUM DECREASED ( 48 FDA reports)
INFLUENZA LIKE ILLNESS ( 48 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 48 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 48 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 48 FDA reports)
VENTRICULAR FIBRILLATION ( 48 FDA reports)
DYSARTHRIA ( 47 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 47 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 47 FDA reports)
GASTROINTESTINAL DISORDER ( 47 FDA reports)
HAEMATEMESIS ( 47 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 47 FDA reports)
PANCREATITIS ( 47 FDA reports)
SINUS DISORDER ( 47 FDA reports)
STOMATITIS ( 47 FDA reports)
CARDIOGENIC SHOCK ( 46 FDA reports)
LEUKOPENIA ( 46 FDA reports)
OROPHARYNGEAL PAIN ( 46 FDA reports)
ORTHOPNOEA ( 46 FDA reports)
PNEUMONITIS ( 46 FDA reports)
SKIN TIGHTNESS ( 46 FDA reports)
DELIRIUM ( 45 FDA reports)
DISTURBANCE IN ATTENTION ( 45 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 45 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 45 FDA reports)
TOOTHACHE ( 45 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 44 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 44 FDA reports)
DRUG TOXICITY ( 44 FDA reports)
DRY SKIN ( 44 FDA reports)
DYSKINESIA ( 44 FDA reports)
RESPIRATORY DISORDER ( 44 FDA reports)
ULCER ( 44 FDA reports)
ADVERSE EVENT ( 43 FDA reports)
ANAPHYLACTIC REACTION ( 43 FDA reports)
BLOOD POTASSIUM DECREASED ( 43 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 43 FDA reports)
DRUG EFFECT DECREASED ( 43 FDA reports)
FLUSHING ( 43 FDA reports)
HEAD INJURY ( 43 FDA reports)
PSEUDOMONAS INFECTION ( 43 FDA reports)
PULMONARY FIBROSIS ( 43 FDA reports)
SOCIAL PROBLEM ( 43 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 43 FDA reports)
SYNOVIAL CYST ( 43 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 43 FDA reports)
BLOOD CALCIUM DECREASED ( 42 FDA reports)
DEFORMITY ( 42 FDA reports)
LOBAR PNEUMONIA ( 42 FDA reports)
NEPHROLITHIASIS ( 42 FDA reports)
RASH GENERALISED ( 42 FDA reports)
RASH PRURITIC ( 42 FDA reports)
FUNGAL INFECTION ( 41 FDA reports)
HAEMATOCHEZIA ( 41 FDA reports)
HEPATIC STEATOSIS ( 41 FDA reports)
JAUNDICE ( 41 FDA reports)
PULSE ABSENT ( 41 FDA reports)
SCAR ( 41 FDA reports)
SKIN DISORDER ( 41 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 40 FDA reports)
OEDEMA MOUTH ( 40 FDA reports)
RENAL CYST ( 40 FDA reports)
BRONCHITIS CHRONIC ( 39 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 39 FDA reports)
COGNITIVE DISORDER ( 39 FDA reports)
DEMENTIA ( 39 FDA reports)
DILATATION VENTRICULAR ( 39 FDA reports)
FLATULENCE ( 39 FDA reports)
INFLAMMATION ( 39 FDA reports)
NERVOUS SYSTEM DISORDER ( 39 FDA reports)
PNEUMOTHORAX ( 39 FDA reports)
RESPIRATORY TRACT CONGESTION ( 39 FDA reports)
SKIN DISCOLOURATION ( 39 FDA reports)
BIPOLAR DISORDER ( 38 FDA reports)
BLOOD GLUCOSE DECREASED ( 38 FDA reports)
BREAST CANCER ( 38 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 38 FDA reports)
FAECAL INCONTINENCE ( 38 FDA reports)
ILEUS ( 38 FDA reports)
JOINT STIFFNESS ( 38 FDA reports)
METABOLIC ACIDOSIS ( 38 FDA reports)
SKIN HYPERTROPHY ( 38 FDA reports)
CORONARY ARTERY OCCLUSION ( 37 FDA reports)
DEAFNESS ( 37 FDA reports)
EYE DISORDER ( 37 FDA reports)
HEPATIC ENZYME INCREASED ( 37 FDA reports)
HYPOCALCAEMIA ( 37 FDA reports)
OFF LABEL USE ( 37 FDA reports)
OSTEOSCLEROSIS ( 37 FDA reports)
RENAL DISORDER ( 37 FDA reports)
SQUAMOUS CELL CARCINOMA ( 37 FDA reports)
ANGINA UNSTABLE ( 36 FDA reports)
CEREBRAL INFARCTION ( 36 FDA reports)
DEVICE MALFUNCTION ( 36 FDA reports)
EXCORIATION ( 36 FDA reports)
FEBRILE NEUTROPENIA ( 36 FDA reports)
GINGIVAL BLEEDING ( 36 FDA reports)
HYPOPHAGIA ( 36 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 36 FDA reports)
SKIN LACERATION ( 36 FDA reports)
TROPONIN INCREASED ( 36 FDA reports)
AGGRESSION ( 35 FDA reports)
DIASTOLIC DYSFUNCTION ( 35 FDA reports)
DIVERTICULITIS ( 35 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 35 FDA reports)
ERECTILE DYSFUNCTION ( 35 FDA reports)
IRON DEFICIENCY ANAEMIA ( 35 FDA reports)
RECTAL POLYP ( 35 FDA reports)
RHONCHI ( 35 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 35 FDA reports)
BASAL CELL CARCINOMA ( 34 FDA reports)
BLOOD POTASSIUM INCREASED ( 34 FDA reports)
FAILURE TO THRIVE ( 34 FDA reports)
FEMUR FRACTURE ( 34 FDA reports)
GASTROENTERITIS ( 34 FDA reports)
HIP FRACTURE ( 34 FDA reports)
LYMPHOMA ( 34 FDA reports)
PANIC ATTACK ( 34 FDA reports)
PHARYNGEAL OEDEMA ( 34 FDA reports)
PNEUMONIA ASPIRATION ( 34 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 34 FDA reports)
RENAL INJURY ( 34 FDA reports)
SCOLIOSIS ( 34 FDA reports)
SUBCUTANEOUS NODULE ( 34 FDA reports)
TOOTH LOSS ( 34 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 33 FDA reports)
DISCOMFORT ( 33 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 33 FDA reports)
SINUS BRADYCARDIA ( 33 FDA reports)
SKIN INDURATION ( 33 FDA reports)
SKIN ULCER ( 33 FDA reports)
TOOTH ABSCESS ( 33 FDA reports)
VENOUS THROMBOSIS ( 33 FDA reports)
ABSCESS JAW ( 32 FDA reports)
AORTIC ANEURYSM ( 32 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 32 FDA reports)
CHEST X-RAY ABNORMAL ( 32 FDA reports)
FAMILY STRESS ( 32 FDA reports)
FLANK PAIN ( 32 FDA reports)
GINGIVITIS ( 32 FDA reports)
HYPOVOLAEMIA ( 32 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 32 FDA reports)
MENISCUS LESION ( 32 FDA reports)
METASTASES TO LUNG ( 32 FDA reports)
PARANOIA ( 32 FDA reports)
RESTLESS LEGS SYNDROME ( 32 FDA reports)
SHOCK ( 32 FDA reports)
SPINAL DISORDER ( 32 FDA reports)
BODY TEMPERATURE INCREASED ( 31 FDA reports)
CYSTITIS ( 31 FDA reports)
DEVICE RELATED INFECTION ( 31 FDA reports)
EDENTULOUS ( 31 FDA reports)
GALLBLADDER DISORDER ( 31 FDA reports)
INJECTION SITE ERYTHEMA ( 31 FDA reports)
JOINT SPRAIN ( 31 FDA reports)
RASH MACULAR ( 31 FDA reports)
SPLENOMEGALY ( 31 FDA reports)
THERAPY NON-RESPONDER ( 31 FDA reports)
WALKING AID USER ( 31 FDA reports)
ANAPHYLACTIC SHOCK ( 30 FDA reports)
APHASIA ( 30 FDA reports)
BACTERIAL INFECTION ( 30 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 30 FDA reports)
DRUG ADMINISTRATION ERROR ( 30 FDA reports)
DYSPNOEA EXACERBATED ( 30 FDA reports)
ESCHERICHIA INFECTION ( 30 FDA reports)
FLUID OVERLOAD ( 30 FDA reports)
GLAUCOMA ( 30 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 30 FDA reports)
LIVER DISORDER ( 30 FDA reports)
MULTIPLE SCLEROSIS ( 30 FDA reports)
PERIPHERAL ISCHAEMIA ( 30 FDA reports)
POLYP ( 30 FDA reports)
PROSTATE CANCER ( 30 FDA reports)
PROTEINURIA ( 30 FDA reports)
RESPIRATORY ACIDOSIS ( 30 FDA reports)
RHABDOMYOLYSIS ( 30 FDA reports)
STEVENS-JOHNSON SYNDROME ( 30 FDA reports)
TENDON RUPTURE ( 30 FDA reports)
ABDOMINAL PAIN LOWER ( 29 FDA reports)
ABSCESS ORAL ( 29 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 29 FDA reports)
BACK DISORDER ( 29 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 29 FDA reports)
BLOOD CHLORIDE DECREASED ( 29 FDA reports)
COR PULMONALE ( 29 FDA reports)
ECZEMA ( 29 FDA reports)
GINGIVAL INFECTION ( 29 FDA reports)
GINGIVAL PAIN ( 29 FDA reports)
HAEMODIALYSIS ( 29 FDA reports)
HEART RATE DECREASED ( 29 FDA reports)
HYPERCALCAEMIA ( 29 FDA reports)
HYPERKERATOSIS ( 29 FDA reports)
LARYNGITIS ( 29 FDA reports)
PERIODONTITIS ( 29 FDA reports)
SKIN LESION ( 29 FDA reports)
ACUTE PRERENAL FAILURE ( 28 FDA reports)
AORTIC STENOSIS ( 28 FDA reports)
CHROMATURIA ( 28 FDA reports)
DIABETIC NEUROPATHY ( 28 FDA reports)
DIALYSIS ( 28 FDA reports)
DIVERTICULUM INTESTINAL ( 28 FDA reports)
EAR PAIN ( 28 FDA reports)
HEPATOMEGALY ( 28 FDA reports)
HOT FLUSH ( 28 FDA reports)
ILEUS PARALYTIC ( 28 FDA reports)
INADEQUATE ANALGESIA ( 28 FDA reports)
INTESTINAL OBSTRUCTION ( 28 FDA reports)
IRRITABILITY ( 28 FDA reports)
MOUTH ULCERATION ( 28 FDA reports)
PALLOR ( 28 FDA reports)
POST PROCEDURAL COMPLICATION ( 28 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 28 FDA reports)
RHINITIS ALLERGIC ( 28 FDA reports)
WOUND INFECTION ( 28 FDA reports)
ACTINOMYCOSIS ( 27 FDA reports)
ADVERSE DRUG REACTION ( 27 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 27 FDA reports)
BREATH SOUNDS ABNORMAL ( 27 FDA reports)
CACHEXIA ( 27 FDA reports)
CARPAL TUNNEL SYNDROME ( 27 FDA reports)
CONJUNCTIVITIS ( 27 FDA reports)
HYPERVENTILATION ( 27 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 27 FDA reports)
JAW FRACTURE ( 27 FDA reports)
RIGHT VENTRICULAR FAILURE ( 27 FDA reports)
TOOTH FRACTURE ( 27 FDA reports)
UROSEPSIS ( 27 FDA reports)
VENTRICULAR DYSFUNCTION ( 27 FDA reports)
AORTIC VALVE SCLEROSIS ( 26 FDA reports)
APHONIA ( 26 FDA reports)
ASPIRATION ( 26 FDA reports)
CHRONIC SINUSITIS ( 26 FDA reports)
CIRCULATORY COLLAPSE ( 26 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 26 FDA reports)
ECCHYMOSIS ( 26 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 26 FDA reports)
INJECTION SITE PAIN ( 26 FDA reports)
JOINT CONTRACTURE ( 26 FDA reports)
KYPHOSIS ( 26 FDA reports)
LACERATION ( 26 FDA reports)
LUNG CONSOLIDATION ( 26 FDA reports)
MITRAL VALVE DISEASE ( 26 FDA reports)
MOVEMENT DISORDER ( 26 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 26 FDA reports)
PEPTIC ULCER ( 26 FDA reports)
PLEURAL FIBROSIS ( 26 FDA reports)
RADICULOPATHY ( 26 FDA reports)
RHINITIS ( 26 FDA reports)
STRESS FRACTURE ( 26 FDA reports)
TENDERNESS ( 26 FDA reports)
THIRST ( 26 FDA reports)
THROAT TIGHTNESS ( 26 FDA reports)
VISUAL ACUITY REDUCED ( 26 FDA reports)
BLEPHARITIS ( 25 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 25 FDA reports)
BREAST CANCER FEMALE ( 25 FDA reports)
DUODENITIS ( 25 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 25 FDA reports)
FIBROMYALGIA ( 25 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 25 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 25 FDA reports)
INJECTION SITE HAEMORRHAGE ( 25 FDA reports)
JOINT DISLOCATION ( 25 FDA reports)
LACTIC ACIDOSIS ( 25 FDA reports)
MUCOSAL INFLAMMATION ( 25 FDA reports)
NOCTURIA ( 25 FDA reports)
OESOPHAGITIS ( 25 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 25 FDA reports)
PRIMARY SEQUESTRUM ( 25 FDA reports)
RESUSCITATION ( 25 FDA reports)
SICK SINUS SYNDROME ( 25 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 25 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 25 FDA reports)
SWOLLEN TONGUE ( 25 FDA reports)
ATRIAL TACHYCARDIA ( 24 FDA reports)
CORONARY ARTERY STENOSIS ( 24 FDA reports)
DEPRESSED MOOD ( 24 FDA reports)
DISEASE RECURRENCE ( 24 FDA reports)
DRUG INTOLERANCE ( 24 FDA reports)
DYSLIPIDAEMIA ( 24 FDA reports)
GASTRIC DISORDER ( 24 FDA reports)
GYNAECOMASTIA ( 24 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 24 FDA reports)
HEPATITIS ( 24 FDA reports)
HYPERTHYROIDISM ( 24 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 24 FDA reports)
METASTASES TO LIVER ( 24 FDA reports)
NEURALGIA ( 24 FDA reports)
PROTEIN URINE PRESENT ( 24 FDA reports)
PRURITUS GENERALISED ( 24 FDA reports)
PULMONARY GRANULOMA ( 24 FDA reports)
STATUS ASTHMATICUS ( 24 FDA reports)
ANKLE FRACTURE ( 23 FDA reports)
DEAFNESS NEUROSENSORY ( 23 FDA reports)
DENTAL PULP DISORDER ( 23 FDA reports)
DRUG DOSE OMISSION ( 23 FDA reports)
ENDODONTIC PROCEDURE ( 23 FDA reports)
EYE SWELLING ( 23 FDA reports)
FACE OEDEMA ( 23 FDA reports)
FEELING COLD ( 23 FDA reports)
FEELING HOT ( 23 FDA reports)
FIBROSIS ( 23 FDA reports)
FOETAL DISTRESS SYNDROME ( 23 FDA reports)
GOITRE ( 23 FDA reports)
HYPERSOMNIA ( 23 FDA reports)
HYPOKINESIA ( 23 FDA reports)
HYPOMAGNESAEMIA ( 23 FDA reports)
IRRITABLE BOWEL SYNDROME ( 23 FDA reports)
LABORATORY TEST ABNORMAL ( 23 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 23 FDA reports)
ORAL DISORDER ( 23 FDA reports)
PRESYNCOPE ( 23 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
VENTRICULAR HYPOKINESIA ( 23 FDA reports)
ACUTE CORONARY SYNDROME ( 22 FDA reports)
ADRENAL INSUFFICIENCY ( 22 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 22 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 22 FDA reports)
CRYING ( 22 FDA reports)
DECUBITUS ULCER ( 22 FDA reports)
DENTAL FISTULA ( 22 FDA reports)
ENTEROCOCCAL INFECTION ( 22 FDA reports)
EXTRASYSTOLES ( 22 FDA reports)
FAECES DISCOLOURED ( 22 FDA reports)
FEELING JITTERY ( 22 FDA reports)
HAEMOLYTIC ANAEMIA ( 22 FDA reports)
HEPATIC ENCEPHALOPATHY ( 22 FDA reports)
HEPATIC LESION ( 22 FDA reports)
HYPERTENSIVE HEART DISEASE ( 22 FDA reports)
INCONTINENCE ( 22 FDA reports)
INTERMITTENT CLAUDICATION ( 22 FDA reports)
KLEBSIELLA INFECTION ( 22 FDA reports)
LIMB INJURY ( 22 FDA reports)
LUMBAR SPINAL STENOSIS ( 22 FDA reports)
MITRAL VALVE CALCIFICATION ( 22 FDA reports)
MOTOR DYSFUNCTION ( 22 FDA reports)
MYELODYSPLASTIC SYNDROME ( 22 FDA reports)
MYOCLONUS ( 22 FDA reports)
NEUROGENIC BLADDER ( 22 FDA reports)
NEUTROPENIC SEPSIS ( 22 FDA reports)
PANCREATITIS ACUTE ( 22 FDA reports)
PLEURITIC PAIN ( 22 FDA reports)
RESTLESSNESS ( 22 FDA reports)
TACHYCARDIA FOETAL ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
ANEURYSM ( 21 FDA reports)
CHONDROMALACIA ( 21 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 21 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 21 FDA reports)
COLD SWEAT ( 21 FDA reports)
CREPITATIONS ( 21 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 21 FDA reports)
DILATATION ATRIAL ( 21 FDA reports)
ELECTROLYTE IMBALANCE ( 21 FDA reports)
HYPERCAPNIA ( 21 FDA reports)
HYPOVENTILATION ( 21 FDA reports)
INFUSION RELATED REACTION ( 21 FDA reports)
JOINT INJURY ( 21 FDA reports)
NECK INJURY ( 21 FDA reports)
ORAL INFECTION ( 21 FDA reports)
PLATELET COUNT INCREASED ( 21 FDA reports)
RENAL TUBULAR NECROSIS ( 21 FDA reports)
SEQUESTRECTOMY ( 21 FDA reports)
SUDDEN DEATH ( 21 FDA reports)
TRANSAMINASES INCREASED ( 21 FDA reports)
VISUAL DISTURBANCE ( 21 FDA reports)
AZOTAEMIA ( 20 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 20 FDA reports)
BREAST CANCER METASTATIC ( 20 FDA reports)
BRONCHIAL SECRETION RETENTION ( 20 FDA reports)
CARDIAC VALVE DISEASE ( 20 FDA reports)
COLON CANCER ( 20 FDA reports)
DERMAL CYST ( 20 FDA reports)
DRUG ABUSE ( 20 FDA reports)
DYSSTASIA ( 20 FDA reports)
EAR INFECTION ( 20 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 20 FDA reports)
EXTREMITY CONTRACTURE ( 20 FDA reports)
EYE PAIN ( 20 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 20 FDA reports)
LIVEDO RETICULARIS ( 20 FDA reports)
LOOSE TOOTH ( 20 FDA reports)
MACULAR DEGENERATION ( 20 FDA reports)
MAJOR DEPRESSION ( 20 FDA reports)
MENTAL IMPAIRMENT ( 20 FDA reports)
MYOPATHY ( 20 FDA reports)
NASAL SEPTUM DEVIATION ( 20 FDA reports)
PERIORBITAL HAEMATOMA ( 20 FDA reports)
RHEUMATOID ARTHRITIS ( 20 FDA reports)
SEBORRHOEIC KERATOSIS ( 20 FDA reports)
SKIN FIBROSIS ( 20 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 20 FDA reports)
SPINAL FRACTURE ( 20 FDA reports)
TENDONITIS ( 20 FDA reports)
TONGUE ULCERATION ( 20 FDA reports)
TRIGEMINAL NEURALGIA ( 20 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 20 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 19 FDA reports)
ATAXIA ( 19 FDA reports)
BLADDER CANCER ( 19 FDA reports)
BONE LESION ( 19 FDA reports)
BRONCHITIS ACUTE ( 19 FDA reports)
BRUXISM ( 19 FDA reports)
COLITIS ISCHAEMIC ( 19 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 19 FDA reports)
DYSAESTHESIA ( 19 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 19 FDA reports)
GENERALISED OEDEMA ( 19 FDA reports)
HAEMOTHORAX ( 19 FDA reports)
HYDRONEPHROSIS ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 19 FDA reports)
INGUINAL HERNIA ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
MUSCLE ATROPHY ( 19 FDA reports)
MUSCLE STRAIN ( 19 FDA reports)
MYASTHENIA GRAVIS ( 19 FDA reports)
NO THERAPEUTIC RESPONSE ( 19 FDA reports)
PERIPHERAL COLDNESS ( 19 FDA reports)
POOR QUALITY SLEEP ( 19 FDA reports)
RASH ERYTHEMATOUS ( 19 FDA reports)
SENSITIVITY OF TEETH ( 19 FDA reports)
SENSORY DISTURBANCE ( 19 FDA reports)
SINUS CONGESTION ( 19 FDA reports)
ACCIDENTAL OVERDOSE ( 18 FDA reports)
ACTINIC KERATOSIS ( 18 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 18 FDA reports)
ADENOCARCINOMA ( 18 FDA reports)
AGRANULOCYTOSIS ( 18 FDA reports)
ASTHMATIC CRISIS ( 18 FDA reports)
BARRETT'S OESOPHAGUS ( 18 FDA reports)
BLOOD CULTURE POSITIVE ( 18 FDA reports)
BONE DEBRIDEMENT ( 18 FDA reports)
BRAIN OEDEMA ( 18 FDA reports)
CARDIOPULMONARY FAILURE ( 18 FDA reports)
COLITIS ( 18 FDA reports)
CONDUCTION DISORDER ( 18 FDA reports)
COORDINATION ABNORMAL ( 18 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 18 FDA reports)
FIBRIN D DIMER INCREASED ( 18 FDA reports)
GASTROENTERITIS VIRAL ( 18 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 18 FDA reports)
HOSPITALISATION ( 18 FDA reports)
INTRACRANIAL ANEURYSM ( 18 FDA reports)
ISCHAEMIA ( 18 FDA reports)
LACRIMATION INCREASED ( 18 FDA reports)
METABOLIC ENCEPHALOPATHY ( 18 FDA reports)
METASTATIC NEOPLASM ( 18 FDA reports)
MITRAL VALVE STENOSIS ( 18 FDA reports)
MUSCLE CRAMP ( 18 FDA reports)
NEPHROPATHY ( 18 FDA reports)
NIGHT SWEATS ( 18 FDA reports)
PERIODONTAL DISEASE ( 18 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 18 FDA reports)
PHARYNGITIS ( 18 FDA reports)
PHYSICAL DISABILITY ( 18 FDA reports)
PLASMACYTOMA ( 18 FDA reports)
PROCEDURAL COMPLICATION ( 18 FDA reports)
PURULENT DISCHARGE ( 18 FDA reports)
ROSACEA ( 18 FDA reports)
SINUS HEADACHE ( 18 FDA reports)
SKIN HYPERPIGMENTATION ( 18 FDA reports)
SKIN REACTION ( 18 FDA reports)
STREPTOCOCCAL SEPSIS ( 18 FDA reports)
TOOTH INFECTION ( 18 FDA reports)
ABDOMINAL TENDERNESS ( 17 FDA reports)
ABSCESS DRAINAGE ( 17 FDA reports)
ANXIETY DISORDER ( 17 FDA reports)
AORTIC CALCIFICATION ( 17 FDA reports)
B-CELL LYMPHOMA ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 17 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 17 FDA reports)
CAROTID BRUIT ( 17 FDA reports)
CATHETERISATION CARDIAC ( 17 FDA reports)
CHOKING ( 17 FDA reports)
CHOLECYSTITIS CHRONIC ( 17 FDA reports)
DIFFICULTY IN WALKING ( 17 FDA reports)
DRUG ABUSER ( 17 FDA reports)
DRUG TOLERANCE ( 17 FDA reports)
DRY EYE ( 17 FDA reports)
DUODENAL ULCER ( 17 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 17 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 17 FDA reports)
EMBOLISM ( 17 FDA reports)
FISTULA ( 17 FDA reports)
GINGIVAL SWELLING ( 17 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 17 FDA reports)
GRAND MAL CONVULSION ( 17 FDA reports)
GRANULOMA ( 17 FDA reports)
HEPATIC CIRRHOSIS ( 17 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 17 FDA reports)
LUMBAR RADICULOPATHY ( 17 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 17 FDA reports)
NEOPLASM ( 17 FDA reports)
NEPHROSCLEROSIS ( 17 FDA reports)
ODYNOPHAGIA ( 17 FDA reports)
OSTEOLYSIS ( 17 FDA reports)
PROTEIN TOTAL DECREASED ( 17 FDA reports)
RASH MACULO-PAPULAR ( 17 FDA reports)
REFLUX OESOPHAGITIS ( 17 FDA reports)
SPUTUM CULTURE POSITIVE ( 17 FDA reports)
STRESS SYMPTOMS ( 17 FDA reports)
URINE OUTPUT DECREASED ( 17 FDA reports)
ASPERGILLOSIS ( 16 FDA reports)
CARDIAC FLUTTER ( 16 FDA reports)
CHOLECYSTITIS ( 16 FDA reports)
CHOLECYSTITIS ACUTE ( 16 FDA reports)
COMPLETED SUICIDE ( 16 FDA reports)
CONNECTIVE TISSUE DISORDER ( 16 FDA reports)
DECREASED ACTIVITY ( 16 FDA reports)
ENDOTRACHEAL INTUBATION ( 16 FDA reports)
EXOSTOSIS ( 16 FDA reports)
EYELID OEDEMA ( 16 FDA reports)
FOOT FRACTURE ( 16 FDA reports)
GASTRITIS EROSIVE ( 16 FDA reports)
GROIN PAIN ( 16 FDA reports)
HEPATIC CONGESTION ( 16 FDA reports)
HYPOAESTHESIA FACIAL ( 16 FDA reports)
IMPAIRED DRIVING ABILITY ( 16 FDA reports)
INCREASED BRONCHIAL SECRETION ( 16 FDA reports)
INTESTINAL PERFORATION ( 16 FDA reports)
LOSS OF EMPLOYMENT ( 16 FDA reports)
MECHANICAL VENTILATION ( 16 FDA reports)
MICTURITION URGENCY ( 16 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 16 FDA reports)
OTITIS MEDIA ( 16 FDA reports)
PERITONITIS ( 16 FDA reports)
PULMONARY MASS ( 16 FDA reports)
QUALITY OF LIFE DECREASED ( 16 FDA reports)
RETCHING ( 16 FDA reports)
SKIN ATROPHY ( 16 FDA reports)
SOFT TISSUE DISORDER ( 16 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 16 FDA reports)
TACHYARRHYTHMIA ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
WOUND ( 16 FDA reports)
ABDOMINAL HERNIA ( 15 FDA reports)
ABNORMAL DREAMS ( 15 FDA reports)
AGEUSIA ( 15 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 15 FDA reports)
ANOXIC ENCEPHALOPATHY ( 15 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 15 FDA reports)
BREATH ODOUR ( 15 FDA reports)
CHEST TUBE INSERTION ( 15 FDA reports)
COMPRESSION FRACTURE ( 15 FDA reports)
CORNEAL ABRASION ( 15 FDA reports)
DELUSION ( 15 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 15 FDA reports)
DRY THROAT ( 15 FDA reports)
FEMORAL NECK FRACTURE ( 15 FDA reports)
FLAT AFFECT ( 15 FDA reports)
HAEMOPHILUS INFECTION ( 15 FDA reports)
HEPATIC CYST ( 15 FDA reports)
HEPATOTOXICITY ( 15 FDA reports)
HYPOTHERMIA ( 15 FDA reports)
INJECTION SITE RASH ( 15 FDA reports)
JAUNDICE CHOLESTATIC ( 15 FDA reports)
JOINT CREPITATION ( 15 FDA reports)
LOCALISED INFECTION ( 15 FDA reports)
LOW TURNOVER OSTEOPATHY ( 15 FDA reports)
NODULE ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER ( 15 FDA reports)
OCCULT BLOOD POSITIVE ( 15 FDA reports)
OCULAR HYPERAEMIA ( 15 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 15 FDA reports)
PATHOLOGICAL FRACTURE ( 15 FDA reports)
PETECHIAE ( 15 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 15 FDA reports)
POLYDIPSIA ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
PULMONARY HILUM MASS ( 15 FDA reports)
PUPIL FIXED ( 15 FDA reports)
SHOULDER PAIN ( 15 FDA reports)
SPINAL CORPECTOMY ( 15 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 15 FDA reports)
SUICIDE ATTEMPT ( 15 FDA reports)
TOXIC SKIN ERUPTION ( 15 FDA reports)
TRAUMATIC LUNG INJURY ( 15 FDA reports)
VASCULAR PSEUDOANEURYSM ( 15 FDA reports)
ABNORMAL BEHAVIOUR ( 14 FDA reports)
ABNORMAL FAECES ( 14 FDA reports)
ANGER ( 14 FDA reports)
BIOPSY BONE ABNORMAL ( 14 FDA reports)
BLINDNESS ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 14 FDA reports)
BLOOD PRESSURE ABNORMAL ( 14 FDA reports)
BODY HEIGHT DECREASED ( 14 FDA reports)
BREAST CYST ( 14 FDA reports)
CARDIAC PACEMAKER INSERTION ( 14 FDA reports)
CATARACT OPERATION ( 14 FDA reports)
CERVICAL CORD COMPRESSION ( 14 FDA reports)
CHOKING SENSATION ( 14 FDA reports)
CHOLECYSTECTOMY ( 14 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 14 FDA reports)
ENDOCARDITIS ( 14 FDA reports)
EOSINOPHIL COUNT INCREASED ( 14 FDA reports)
ERUCTATION ( 14 FDA reports)
FACIAL PAIN ( 14 FDA reports)
GLOSSODYNIA ( 14 FDA reports)
HERNIA ( 14 FDA reports)
HYPERPARATHYROIDISM ( 14 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 14 FDA reports)
IRON DEFICIENCY ( 14 FDA reports)
LARYNGEAL OEDEMA ( 14 FDA reports)
LUDWIG ANGINA ( 14 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 14 FDA reports)
MACROGLOSSIA ( 14 FDA reports)
MOOD ALTERED ( 14 FDA reports)
MUSCLE TWITCHING ( 14 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 14 FDA reports)
MYELOMA RECURRENCE ( 14 FDA reports)
MYELOPATHY ( 14 FDA reports)
PORTAL HYPERTENSION ( 14 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 14 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 14 FDA reports)
SINUS OPERATION ( 14 FDA reports)
SKIN FRAGILITY ( 14 FDA reports)
SKIN WARM ( 14 FDA reports)
SNEEZING ( 14 FDA reports)
SPINAL FUSION ACQUIRED ( 14 FDA reports)
TARDIVE DYSKINESIA ( 14 FDA reports)
TENOSYNOVITIS ( 14 FDA reports)
UTERINE CANCER ( 14 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 13 FDA reports)
ATHEROSCLEROSIS ( 13 FDA reports)
BLOOD CALCIUM INCREASED ( 13 FDA reports)
BONE NEOPLASM MALIGNANT ( 13 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 13 FDA reports)
BRAIN INJURY ( 13 FDA reports)
BRONCHIECTASIS ( 13 FDA reports)
CARDIAC TAMPONADE ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 13 FDA reports)
CEREBROVASCULAR DISORDER ( 13 FDA reports)
CERUMEN IMPACTION ( 13 FDA reports)
CLOSTRIDIAL INFECTION ( 13 FDA reports)
COAGULATION TEST ABNORMAL ( 13 FDA reports)
COLLAPSE OF LUNG ( 13 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 13 FDA reports)
DERMATITIS ( 13 FDA reports)
EATING DISORDER ( 13 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 13 FDA reports)
EROSIVE DUODENITIS ( 13 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 13 FDA reports)
HAEMANGIOMA OF LIVER ( 13 FDA reports)
HYPOGONADISM ( 13 FDA reports)
INCISION SITE COMPLICATION ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 13 FDA reports)
JAW DISORDER ( 13 FDA reports)
JOINT EFFUSION ( 13 FDA reports)
LEFT VENTRICULAR FAILURE ( 13 FDA reports)
LIP SWELLING ( 13 FDA reports)
LOWER LIMB FRACTURE ( 13 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 13 FDA reports)
MUSCLE HAEMORRHAGE ( 13 FDA reports)
MUSCLE RIGIDITY ( 13 FDA reports)
MUSCLE TIGHTNESS ( 13 FDA reports)
NEURITIS ( 13 FDA reports)
NEUROPATHY ( 13 FDA reports)
NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
NIKOLSKY'S SIGN ( 13 FDA reports)
NON-CARDIAC CHEST PAIN ( 13 FDA reports)
OPEN REDUCTION OF FRACTURE ( 13 FDA reports)
OSTEITIS ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
PARALYSIS ( 13 FDA reports)
POOR DENTAL CONDITION ( 13 FDA reports)
POSTMENOPAUSE ( 13 FDA reports)
SENSATION OF HEAVINESS ( 13 FDA reports)
SKELETAL INJURY ( 13 FDA reports)
SKIN BURNING SENSATION ( 13 FDA reports)
SKIN CANCER ( 13 FDA reports)
SPINAL FUSION SURGERY ( 13 FDA reports)
STOMACH DISCOMFORT ( 13 FDA reports)
TORSADE DE POINTES ( 13 FDA reports)
VITAMIN D DEFICIENCY ( 13 FDA reports)
ACIDOSIS ( 12 FDA reports)
ALCOHOL POISONING ( 12 FDA reports)
ANURIA ( 12 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
BACK INJURY ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 12 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 12 FDA reports)
BLADDER PROLAPSE ( 12 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
CAESAREAN SECTION ( 12 FDA reports)
CARDIAC OPERATION ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 12 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 12 FDA reports)
CEREBRAL HAEMORRHAGE ( 12 FDA reports)
CERVICAL SPINAL STENOSIS ( 12 FDA reports)
CHARLES BONNET SYNDROME ( 12 FDA reports)
CHEILITIS ( 12 FDA reports)
CHRONIC FATIGUE SYNDROME ( 12 FDA reports)
CUSHING'S SYNDROME ( 12 FDA reports)
CYSTOCELE ( 12 FDA reports)
DEVICE FAILURE ( 12 FDA reports)
EAR NEOPLASM ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 12 FDA reports)
EMBOLIC STROKE ( 12 FDA reports)
EOSINOPHILIA ( 12 FDA reports)
EPICONDYLITIS ( 12 FDA reports)
ESCHERICHIA SEPSIS ( 12 FDA reports)
EYE INFECTION ( 12 FDA reports)
FAECES PALE ( 12 FDA reports)
FIBROMA ( 12 FDA reports)
FRACTURE NONUNION ( 12 FDA reports)
FURUNCLE ( 12 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
GOUT ( 12 FDA reports)
HILAR LYMPHADENOPATHY ( 12 FDA reports)
HYPOPHOSPHATAEMIA ( 12 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 12 FDA reports)
INTESTINAL ISCHAEMIA ( 12 FDA reports)
INTRACARDIAC THROMBUS ( 12 FDA reports)
LARGE INTESTINE PERFORATION ( 12 FDA reports)
LIGAMENT SPRAIN ( 12 FDA reports)
MUSCLE CONTRACTURE ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
PELVIC PAIN ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 12 FDA reports)
POSTNASAL DRIP ( 12 FDA reports)
PROCEDURAL PAIN ( 12 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 12 FDA reports)
PURPURA ( 12 FDA reports)
PYODERMA GANGRENOSUM ( 12 FDA reports)
RASH PAPULAR ( 12 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 12 FDA reports)
RETINAL DETACHMENT ( 12 FDA reports)
RIGHT ATRIAL DILATATION ( 12 FDA reports)
SCHIZOPHRENIA ( 12 FDA reports)
STENT PLACEMENT ( 12 FDA reports)
SUFFOCATION FEELING ( 12 FDA reports)
SUPERINFECTION ( 12 FDA reports)
THROMBOSIS IN DEVICE ( 12 FDA reports)
UTERINE HAEMORRHAGE ( 12 FDA reports)
ANAEMIA POSTOPERATIVE ( 11 FDA reports)
ANGIOEDEMA ( 11 FDA reports)
BLADDER OBSTRUCTION ( 11 FDA reports)
BLINDNESS UNILATERAL ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
BLOOD PH DECREASED ( 11 FDA reports)
BLOOD URINE PRESENT ( 11 FDA reports)
BREAST MASS ( 11 FDA reports)
CEREBRAL ISCHAEMIA ( 11 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 11 FDA reports)
CLOSTRIDIUM COLITIS ( 11 FDA reports)
CONVULSION NEONATAL ( 11 FDA reports)
DEBRIDEMENT ( 11 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 11 FDA reports)
DIABETIC NEPHROPATHY ( 11 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 11 FDA reports)
EXTREMITY NECROSIS ( 11 FDA reports)
FIBULA FRACTURE ( 11 FDA reports)
GINGIVAL RECESSION ( 11 FDA reports)
HAEMOLYSIS ( 11 FDA reports)
HEMIPLEGIA ( 11 FDA reports)
HEPATIC ENZYME ABNORMAL ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
HOARSENESS ( 11 FDA reports)
HYPERBILIRUBINAEMIA ( 11 FDA reports)
HYPOTONIA ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INCREASED TENDENCY TO BRUISE ( 11 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 11 FDA reports)
ISCHAEMIC HEPATITIS ( 11 FDA reports)
JAW OPERATION ( 11 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 11 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 11 FDA reports)
MELANOCYTIC NAEVUS ( 11 FDA reports)
MICROCYTOSIS ( 11 FDA reports)
ORAL SURGERY ( 11 FDA reports)
ORAL TORUS ( 11 FDA reports)
OTITIS MEDIA CHRONIC ( 11 FDA reports)
PERICARDITIS ( 11 FDA reports)
POISONING ( 11 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 11 FDA reports)
PRESBYOPIA ( 11 FDA reports)
PROTEUS INFECTION ( 11 FDA reports)
PSYCHOTIC DISORDER ( 11 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 11 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
RHEUMATIC HEART DISEASE ( 11 FDA reports)
SEDATION ( 11 FDA reports)
SKIN NODULE ( 11 FDA reports)
TALIPES ( 11 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 11 FDA reports)
TENSION ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 11 FDA reports)
VAGINAL HAEMORRHAGE ( 11 FDA reports)
VENOUS INSUFFICIENCY ( 11 FDA reports)
VITAMIN B12 DEFICIENCY ( 11 FDA reports)
WHEELCHAIR USER ( 11 FDA reports)
WOUND SECRETION ( 11 FDA reports)
X-RAY ABNORMAL ( 11 FDA reports)
ABSCESS NECK ( 10 FDA reports)
ACUTE SINUSITIS ( 10 FDA reports)
ADDISON'S DISEASE ( 10 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 10 FDA reports)
ALVEOLAR OSTEITIS ( 10 FDA reports)
ANGIONEUROTIC OEDEMA ( 10 FDA reports)
BEDRIDDEN ( 10 FDA reports)
BLOOD MAGNESIUM DECREASED ( 10 FDA reports)
BLOOD MAGNESIUM INCREASED ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 10 FDA reports)
BONE EROSION ( 10 FDA reports)
BREAST NEOPLASM ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
CERVICOBRACHIAL SYNDROME ( 10 FDA reports)
CLAVICLE FRACTURE ( 10 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
DIABETIC ULCER ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
EPILEPSY ( 10 FDA reports)
FANCONI SYNDROME ( 10 FDA reports)
FISTULA DISCHARGE ( 10 FDA reports)
GASTRIC POLYPS ( 10 FDA reports)
GASTROINTESTINAL PAIN ( 10 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 10 FDA reports)
HYPOREFLEXIA ( 10 FDA reports)
HYPOVOLAEMIC SHOCK ( 10 FDA reports)
INCISION SITE INFECTION ( 10 FDA reports)
INGUINAL MASS ( 10 FDA reports)
KNEE ARTHROPLASTY ( 10 FDA reports)
KYPHOSCOLIOSIS ( 10 FDA reports)
LOCALISED OEDEMA ( 10 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
METASTASES TO LYMPH NODES ( 10 FDA reports)
MUCOUS MEMBRANE DISORDER ( 10 FDA reports)
NERVE COMPRESSION ( 10 FDA reports)
NIGHTMARE ( 10 FDA reports)
NODAL ARRHYTHMIA ( 10 FDA reports)
NOSOCOMIAL INFECTION ( 10 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 10 FDA reports)
ORAL INTAKE REDUCED ( 10 FDA reports)
OXYGEN SUPPLEMENTATION ( 10 FDA reports)
PARTNER STRESS ( 10 FDA reports)
PEAU D'ORANGE ( 10 FDA reports)
PERONEAL NERVE PALSY ( 10 FDA reports)
PHOTOPHOBIA ( 10 FDA reports)
PO2 DECREASED ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 10 FDA reports)
PULMONARY INFARCTION ( 10 FDA reports)
RADICAL MASTECTOMY ( 10 FDA reports)
RECTOCELE ( 10 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 10 FDA reports)
SEPSIS SYNDROME ( 10 FDA reports)
SIALOADENITIS ( 10 FDA reports)
SKIN NECROSIS ( 10 FDA reports)
SPLENIC INFARCTION ( 10 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 10 FDA reports)
TUMOUR NECROSIS ( 10 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 10 FDA reports)
VASCULAR PURPURA ( 10 FDA reports)
WOUND DEHISCENCE ( 10 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 9 FDA reports)
ADRENAL DISORDER ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
APPLICATION SITE IRRITATION ( 9 FDA reports)
ARTERIAL BYPASS OPERATION ( 9 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 9 FDA reports)
BLINDNESS TRANSIENT ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BLOOD PH INCREASED ( 9 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
BONE MARROW TRANSPLANT ( 9 FDA reports)
CARDIAC ASTHMA ( 9 FDA reports)
CAROTID ARTERY DISEASE ( 9 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CULTURE URINE POSITIVE ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
DERMATITIS CONTACT ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
DYSPHORIA ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 9 FDA reports)
EMPYEMA ( 9 FDA reports)
ENDOCARDIAL FIBROSIS ( 9 FDA reports)
EXPOSED BONE IN JAW ( 9 FDA reports)
EYE IRRITATION ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FEMORAL ARTERY OCCLUSION ( 9 FDA reports)
GASTRIC HAEMORRHAGE ( 9 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 9 FDA reports)
GLOSSITIS ( 9 FDA reports)
HAEMORRHAGIC ANAEMIA ( 9 FDA reports)
HAND FRACTURE ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HEPATITIS ACUTE ( 9 FDA reports)
HEPATITIS TOXIC ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
HYPERURICAEMIA ( 9 FDA reports)
HYPOAESTHESIA ORAL ( 9 FDA reports)
INFARCTION ( 9 FDA reports)
JOINT INSTABILITY ( 9 FDA reports)
JUGULAR VEIN THROMBOSIS ( 9 FDA reports)
LARYNGEAL CANCER ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
LUNG HYPERINFLATION ( 9 FDA reports)
LYMPHOPENIA ( 9 FDA reports)
MENORRHAGIA ( 9 FDA reports)
MIDDLE INSOMNIA ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
NEURODERMATITIS ( 9 FDA reports)
NODAL RHYTHM ( 9 FDA reports)
ORAL CAVITY FISTULA ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
OTITIS EXTERNA ( 9 FDA reports)
PANCREATIC DISORDER ( 9 FDA reports)
PAPILLOEDEMA ( 9 FDA reports)
PAPILLOMA ( 9 FDA reports)
PARAESTHESIA ORAL ( 9 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 9 FDA reports)
PHLEBITIS ( 9 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 9 FDA reports)
POLYSUBSTANCE ABUSE ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
PYURIA ( 9 FDA reports)
QRS AXIS ABNORMAL ( 9 FDA reports)
RENAL ARTERY STENOSIS ( 9 FDA reports)
RESPIRATORY DEPRESSION ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
SACROILIITIS ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SINUSITIS FUNGAL ( 9 FDA reports)
SUICIDAL BEHAVIOUR ( 9 FDA reports)
TEMPERATURE INTOLERANCE ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 9 FDA reports)
TOBACCO ABUSE ( 9 FDA reports)
TOE DEFORMITY ( 9 FDA reports)
TYPE 1 DIABETES MELLITUS ( 9 FDA reports)
URINARY HESITATION ( 9 FDA reports)
VAGINAL INFECTION ( 9 FDA reports)
VARICES OESOPHAGEAL ( 9 FDA reports)
VASCULAR INSUFFICIENCY ( 9 FDA reports)
VENTRICULAR ARRHYTHMIA ( 9 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 9 FDA reports)
VIITH NERVE PARALYSIS ( 9 FDA reports)
ABDOMINAL SEPSIS ( 8 FDA reports)
ALVEOLOPLASTY ( 8 FDA reports)
APLASIA PURE RED CELL ( 8 FDA reports)
APPENDIX DISORDER ( 8 FDA reports)
ARTERIOVENOUS FISTULA ( 8 FDA reports)
ASPHYXIA ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
BILE DUCT OBSTRUCTION ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BRADYARRHYTHMIA ( 8 FDA reports)
BUNDLE BRANCH BLOCK ( 8 FDA reports)
CALCULUS URETERIC ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 8 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
ENCEPHALOMALACIA ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
FEELING DRUNK ( 8 FDA reports)
GRIP STRENGTH DECREASED ( 8 FDA reports)
HAEMANGIOMA ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
HUNGER ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
HYPERPLASIA ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
ILEITIS ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INGUINAL HERNIA REPAIR ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
ISCHAEMIC STROKE ( 8 FDA reports)
LIBIDO DECREASED ( 8 FDA reports)
LIP EROSION ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
LYMPHOEDEMA ( 8 FDA reports)
MANIA ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
MONOCLONAL GAMMOPATHY ( 8 FDA reports)
MUSCLE FATIGUE ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
OESOPHAGEAL SPASM ( 8 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
ONYCHOMYCOSIS ( 8 FDA reports)
OPEN WOUND ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 8 FDA reports)
PSYCHIATRIC SYMPTOM ( 8 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
RENAL CELL CARCINOMA ( 8 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 8 FDA reports)
RESPIRATORY ALKALOSIS ( 8 FDA reports)
SERUM FERRITIN INCREASED ( 8 FDA reports)
SKIN DEPIGMENTATION ( 8 FDA reports)
STASIS DERMATITIS ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
TEARFULNESS ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
THYROID DISORDER ( 8 FDA reports)
TONGUE NEOPLASM ( 8 FDA reports)
TOOTH DEPOSIT ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
VITREOUS FLOATERS ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
WOUND DRAINAGE ( 8 FDA reports)
WRIST FRACTURE ( 8 FDA reports)
ACNE ( 7 FDA reports)
ALCOHOL ABUSE ( 7 FDA reports)
ALLERGY TO CHEMICALS ( 7 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APPENDICITIS ( 7 FDA reports)
APPLICATION SITE ERYTHEMA ( 7 FDA reports)
ARTERIAL STENOSIS ( 7 FDA reports)
ARTHROPOD BITE ( 7 FDA reports)
ASEPTIC NECROSIS BONE ( 7 FDA reports)
ATRIAL SEPTAL DEFECT ( 7 FDA reports)
ATROPHY ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BLOOD BICARBONATE DECREASED ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 7 FDA reports)
BODY TEMPERATURE DECREASED ( 7 FDA reports)
BONE LOSS ( 7 FDA reports)
BREAST PAIN ( 7 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 7 FDA reports)
CARDIOVERSION ( 7 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 7 FDA reports)
CARTILAGE INJURY ( 7 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
COLECTOMY ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
DIABETIC RETINOPATHY ( 7 FDA reports)
DIAPHRAGMATIC DISORDER ( 7 FDA reports)
DIVERTICULAR PERFORATION ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
EXANTHEM ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
FISTULA REPAIR ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMOCHROMATOSIS ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HALLUCINATION, VISUAL ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HEPATIC VEIN THROMBOSIS ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
HOSPICE CARE ( 7 FDA reports)
HYPERCOAGULATION ( 7 FDA reports)
HYPERTHERMIA ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
IMMOBILE ( 7 FDA reports)
INCISIONAL HERNIA ( 7 FDA reports)
INDURATION ( 7 FDA reports)
INJECTION SITE HAEMATOMA ( 7 FDA reports)
INJECTION SITE REACTION ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
INTRAOCULAR LENS IMPLANT ( 7 FDA reports)
KNEE OPERATION ( 7 FDA reports)
LABYRINTHITIS ( 7 FDA reports)
LARGE INTESTINAL ULCER ( 7 FDA reports)
LARYNGOSPASM ( 7 FDA reports)
LIFE EXPECTANCY SHORTENED ( 7 FDA reports)
LIPID METABOLISM DISORDER ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
METABOLIC ALKALOSIS ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
METASTATIC PAIN ( 7 FDA reports)
MITRAL VALVE PROLAPSE ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
NAIL BED TENDERNESS ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
NEUROMYOPATHY ( 7 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OPEN ANGLE GLAUCOMA ( 7 FDA reports)
ORAL FUNGAL INFECTION ( 7 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 7 FDA reports)
ORAL PRURITUS ( 7 FDA reports)
OSTEOCHONDROSIS ( 7 FDA reports)
PATELLA FRACTURE ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
PERSONALITY DISORDER ( 7 FDA reports)
PLEURISY ( 7 FDA reports)
PNEUMONIA KLEBSIELLA ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
PULMONARY TOXICITY ( 7 FDA reports)
PUPILS UNEQUAL ( 7 FDA reports)
PYODERMA ( 7 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
SEXUAL DYSFUNCTION ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
UNDERDOSE ( 7 FDA reports)
VEIN DISORDER ( 7 FDA reports)
VENA CAVA FILTER INSERTION ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VENOUS THROMBOSIS LIMB ( 7 FDA reports)
WOUND HAEMORRHAGE ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
ALCOHOL USE ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
AORTIC DISORDER ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
BIPOLAR I DISORDER ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 6 FDA reports)
BONE FISTULA ( 6 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 6 FDA reports)
BREATH SOUNDS DECREASED ( 6 FDA reports)
BRONCHIAL CARCINOMA ( 6 FDA reports)
BRONCHIAL HYPERACTIVITY ( 6 FDA reports)
BRONCHITIS VIRAL ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 6 FDA reports)
CALCINOSIS ( 6 FDA reports)
CARDIAC ANEURYSM ( 6 FDA reports)
CARDIAC HYPERTROPHY ( 6 FDA reports)
CARDIORENAL SYNDROME ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CATARACT NUCLEAR ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CATHETER SITE HAEMORRHAGE ( 6 FDA reports)
CATHETERISATION VENOUS ( 6 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
COGNITIVE DETERIORATION ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CUSHINGOID ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
DENTAL IMPLANTATION ( 6 FDA reports)
DERMATITIS ALLERGIC ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DIZZINESS POSTURAL ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DRUG TOLERANCE INCREASED ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENTERITIS ( 6 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 6 FDA reports)
EOSINOPHIL COUNT DECREASED ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
ETHMOID SINUS SURGERY ( 6 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
EYELID DISORDER ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 6 FDA reports)
FLASHBACK ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
FRACTURE ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GASTRIC DILATATION ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEARING IMPAIRED ( 6 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERKINESIA ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
IMPAIRED SELF-CARE ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INJECTION SITE COLDNESS ( 6 FDA reports)
INJECTION SITE DISCOMFORT ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INTESTINAL DILATATION ( 6 FDA reports)
JUGULAR VEIN DISTENSION ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LABILE BLOOD PRESSURE ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
LOSS OF LIBIDO ( 6 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 6 FDA reports)
MARROW HYPERPLASIA ( 6 FDA reports)
MAXILLOFACIAL OPERATION ( 6 FDA reports)
MENIERE'S DISEASE ( 6 FDA reports)
MENINGITIS ASEPTIC ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
MUSCLE SPASTICITY ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
ONYCHALGIA ( 6 FDA reports)
ORGAN FAILURE ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
OROANTRAL FISTULA ( 6 FDA reports)
OROPHARYNGEAL SWELLING ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PAIN OF SKIN ( 6 FDA reports)
PALATAL DISORDER ( 6 FDA reports)
PATHOGEN RESISTANCE ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PELVIC FRACTURE ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PLASMAPHERESIS ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POTENTIATING DRUG INTERACTION ( 6 FDA reports)
PRODUCT TASTE ABNORMAL ( 6 FDA reports)
PROLAPSE REPAIR ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
RASH VESICULAR ( 6 FDA reports)
RECTAL PROLAPSE ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
SCAB ( 6 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SENSORY LEVEL ABNORMAL ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
SERUM SICKNESS ( 6 FDA reports)
SINUS ANTROSTOMY ( 6 FDA reports)
SPUTUM PURULENT ( 6 FDA reports)
STRESS CARDIOMYOPATHY ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SYSTEMIC CANDIDA ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
THYROID NEOPLASM ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TRANSFUSION ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
URINE KETONE BODY PRESENT ( 6 FDA reports)
UTERINE DISORDER ( 6 FDA reports)
UTERINE LEIOMYOMA ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VASCULAR INJURY ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACANTHOSIS ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ADNEXA UTERI CYST ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
APATHY ( 5 FDA reports)
ASCITES INFECTION ( 5 FDA reports)
BALANITIS ( 5 FDA reports)
BETA GLOBULIN INCREASED ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 5 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN STEM STROKE ( 5 FDA reports)
BREAST HAEMATOMA ( 5 FDA reports)
BRONCHIAL IRRITATION ( 5 FDA reports)
BRONCHIAL OBSTRUCTION ( 5 FDA reports)
BUTTOCK PAIN ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CHAPPED LIPS ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHOLESTATIC LIVER INJURY ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CYST ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DIET REFUSAL ( 5 FDA reports)
DISEASE COMPLICATION ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
ENTEROCOCCAL SEPSIS ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 5 FDA reports)
GASTROINTESTINAL PERFORATION ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
HALO VISION ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEART BLOCK CONGENITAL ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HEPATORENAL FAILURE ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HYPERPHOSPHATAEMIA ( 5 FDA reports)
HYPERTHERMIA MALIGNANT ( 5 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
IMPETIGO ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INCREASED APPETITE ( 5 FDA reports)
INFUSION SITE HAEMORRHAGE ( 5 FDA reports)
INITIAL INSOMNIA ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
KETOACIDOSIS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
LOCALISED OSTEOARTHRITIS ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
METASTASES TO MENINGES ( 5 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 5 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MULTIPLE ALLERGIES ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NEUROTOXICITY ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 5 FDA reports)
OPEN FRACTURE ( 5 FDA reports)
OSTEOARTHROPATHY ( 5 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERIPHERAL EMBOLISM ( 5 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 5 FDA reports)
PICKWICKIAN SYNDROME ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
POLYARTERITIS NODOSA ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
PSYCHOLOGICAL TRAUMA ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SEROMA ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SINUS ARRHYTHMIA ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SPONDYLOLISTHESIS ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
STRESS URINARY INCONTINENCE ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
SYNOVITIS ( 5 FDA reports)
TACHYPHRENIA ( 5 FDA reports)
TERMINAL STATE ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TOBACCO USER ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TOOTH IMPACTED ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRANSFUSION REACTION ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TREATMENT FAILURE ( 5 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 5 FDA reports)
UMBILICAL CORD AROUND NECK ( 5 FDA reports)
UMBILICAL HERNIA ( 5 FDA reports)
UNDERWEIGHT ( 5 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 5 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VENTRICULAR FAILURE ( 5 FDA reports)
VERTIGO CNS ORIGIN ( 5 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 4 FDA reports)
ABDOMINAL INFECTION ( 4 FDA reports)
ACCIDENT ( 4 FDA reports)
ADENOIDECTOMY ( 4 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ALBUMIN URINE PRESENT ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
ANORECTAL DISCOMFORT ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD PRESSURE ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BONE MARROW TOXICITY ( 4 FDA reports)
BRADYCARDIA FOETAL ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BULLOUS LUNG DISEASE ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
CAMPYLOBACTER INFECTION ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CATHETER PLACEMENT ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
COR PULMONALE CHRONIC ( 4 FDA reports)
CORNEAL DYSTROPHY ( 4 FDA reports)
COSTOCHONDRITIS ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DROOLING ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
EARLY SATIETY ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
FEELING OF DESPAIR ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOOD ALLERGY ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEART VALVE STENOSIS ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HOMICIDAL IDEATION ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPOTONIC URINARY BLADDER ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 4 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INTENTIONAL SELF-INJURY ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
INTESTINAL POLYP ( 4 FDA reports)
KERATECTOMY ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LABILE HYPERTENSION ( 4 FDA reports)
LARYNGEAL ULCERATION ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LOCAL REACTION ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
MAGNESIUM DEFICIENCY ( 4 FDA reports)
MALIGNANT TUMOUR EXCISION ( 4 FDA reports)
MALOCCLUSION ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
METASTASES TO ADRENALS ( 4 FDA reports)
METASTASES TO MUSCLE ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MITRAL VALVE REPLACEMENT ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MYCOSIS FUNGOIDES ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
NAIL DISORDER ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEISSERIA INFECTION ( 4 FDA reports)
NEOPLASM RECURRENCE ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
PROCEDURAL NAUSEA ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 4 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
PULSE ABNORMAL ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RADIATION PNEUMONITIS ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
REFRACTION DISORDER ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RHYTHM IDIOVENTRICULAR ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SKIN HYPOPIGMENTATION ( 4 FDA reports)
SKIN INFECTION ( 4 FDA reports)
SNORING ( 4 FDA reports)
SOFT TISSUE INJURY ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TUMOUR FLARE ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VITAMIN K DEFICIENCY ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
VOCAL CORD PARALYSIS ( 4 FDA reports)
VOCAL CORD THICKENING ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
ABDOMINAL WALL INFECTION ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ACARODERMATITIS ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
ANAL EROSION ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
APPLICATION SITE EROSION ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLADDER DYSFUNCTION ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BONE OPERATION ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHOPLEURAL FISTULA ( 3 FDA reports)
BRONCHOSPASM PARADOXICAL ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CAPILLARY FRAGILITY ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CARDITIS ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CERVICAL MYELOPATHY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
COARCTATION OF THE AORTA ( 3 FDA reports)
COLON CANCER STAGE IV ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 3 FDA reports)
DENTAL PROSTHESIS USER ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DEVICE INEFFECTIVE ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DUBIN-JOHNSON SYNDROME ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FLAIL CHEST ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOETAL HEART RATE DECREASED ( 3 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GINGIVAL ERYTHEMA ( 3 FDA reports)
GRAFT DYSFUNCTION ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HEPATIC CALCIFICATION ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HORMONE LEVEL ABNORMAL ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFUSION SITE HAEMATOMA ( 3 FDA reports)
INFUSION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JOINT LOCK ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LDL/HDL RATIO INCREASED ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
METASTASES TO PANCREAS ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NASAL ULCER ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OESOPHAGEAL MASS ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
OROPHARYNGEAL PLAQUE ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
OXYGEN SATURATION INCREASED ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
PANCOAST'S SYNDROME ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PERITONEAL INFECTION ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 3 FDA reports)
PLASMACYTOSIS ( 3 FDA reports)
PNEUMOCONIOSIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROLONGED EXPIRATION ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
RADICULITIS ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SCLERAL HAEMORRHAGE ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCLERODACTYLIA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SHONE COMPLEX ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SLEEP-RELATED EATING DISORDER ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC RUPTURE ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
STRESS INCONTINENCE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
VIRAL RHINITIS ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WEANING FAILURE ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANOREXIA NERVOSA ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURA ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BASAL GANGLION DEGENERATION ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BUNION ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC PSEUDOANEURYSM ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISBACTERIOSIS ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHROSIS ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRANULOCYTES ABNORMAL ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS B ANTIBODY ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HIP DEFORMITY ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERADRENALISM ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE BRUISING ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LARYNGITIS BACTERIAL ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LARYNGOMALACIA ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIMB PROSTHESIS USER ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MEDIASTINAL SHIFT ( 2 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 2 FDA reports)
MENINGIOMA BENIGN ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
ODONTOGENIC CYST ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OROPHARYNGITIS FUNGAL ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEORADIONECROSIS ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERINEAL FISTULA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PLICA SYNDROME ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POSTOPERATIVE CONSTIPATION ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROLACTINOMA ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUNCTURE SITE REACTION ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCROTAL IRRITATION ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STARING ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VERTEBROPLASTY ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ADENOVIRAL UPPER RESPIRATORY INFECTION ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE EVENT FOLLOWING IMMUNISATION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALBUMIN CSF INCREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTASTHMATIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATHEROSCLEROSIS PROPHYLAXIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY ABDOMINAL WALL ABNORMAL ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD COUNT ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOMALACIA ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CAROTID ANGIOPLASTY ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF NEUTROPHIL COUNT POSITIVE ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC BULLOSIS ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISORDER OF GLOBE ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL CANCER RECURRENT ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EOSINOPHILIC PUSTULOSIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR OF ANIMALS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL CLEFT ( 1 FDA reports)
LARYNGEAL DYSPLASIA ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMIC LYMPHOMA ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METEOROPATHY ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MINERAL SUPPLEMENTATION ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MISCARRIAGE OF PARTNER ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEOPLASM OF ORBIT ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
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NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
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NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
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NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURNAL FEAR ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
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OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
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ORAL DISCHARGE ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTNER'S SYNDROME ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
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PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
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PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
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PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
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PARAKERATOSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
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PARAPLEGIA ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
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PARESIS ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
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PEDAL PULSE ABNORMAL ( 1 FDA reports)
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PELVIC HAEMATOMA ( 1 FDA reports)
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PERICARDIAL RUB ( 1 FDA reports)
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PERNICIOUS ANAEMIA ( 1 FDA reports)
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PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
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PLACENTAL DISORDER ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
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POLYCHONDRITIS ( 1 FDA reports)
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POLYP COLORECTAL ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
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PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
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PRODUCT COUNTERFEIT ( 1 FDA reports)
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PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
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PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
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PUSTULAR PSORIASIS ( 1 FDA reports)
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RADICULITIS CERVICAL ( 1 FDA reports)
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REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
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RECURRING SKIN BOILS ( 1 FDA reports)
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RENAL ANEURYSM ( 1 FDA reports)
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