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

PAIN ( 1195 FDA reports)
ANXIETY ( 960 FDA reports)
NAUSEA ( 917 FDA reports)
DYSPNOEA ( 879 FDA reports)
DIARRHOEA ( 710 FDA reports)
VOMITING ( 694 FDA reports)
INJURY ( 675 FDA reports)
PNEUMONIA ( 605 FDA reports)
PYREXIA ( 589 FDA reports)
ASTHENIA ( 520 FDA reports)
DIZZINESS ( 520 FDA reports)
FATIGUE ( 498 FDA reports)
DEPRESSION ( 473 FDA reports)
PULMONARY EMBOLISM ( 461 FDA reports)
HEADACHE ( 457 FDA reports)
ANAEMIA ( 452 FDA reports)
COUGH ( 443 FDA reports)
CHEST PAIN ( 438 FDA reports)
ABDOMINAL PAIN ( 427 FDA reports)
OEDEMA PERIPHERAL ( 424 FDA reports)
PAIN IN EXTREMITY ( 423 FDA reports)
EMOTIONAL DISTRESS ( 402 FDA reports)
ARTHRALGIA ( 396 FDA reports)
BACK PAIN ( 395 FDA reports)
ABDOMINAL PAIN UPPER ( 387 FDA reports)
DEEP VEIN THROMBOSIS ( 385 FDA reports)
CHOLECYSTITIS CHRONIC ( 377 FDA reports)
DRUG INTERACTION ( 367 FDA reports)
RENAL FAILURE ACUTE ( 363 FDA reports)
HYPOTENSION ( 361 FDA reports)
WEIGHT DECREASED ( 354 FDA reports)
FALL ( 346 FDA reports)
CHOLELITHIASIS ( 331 FDA reports)
DEHYDRATION ( 309 FDA reports)
CONSTIPATION ( 306 FDA reports)
HYPERTENSION ( 296 FDA reports)
RASH ( 296 FDA reports)
DRUG INEFFECTIVE ( 295 FDA reports)
INSOMNIA ( 285 FDA reports)
BRONCHITIS ( 279 FDA reports)
URINARY TRACT INFECTION ( 279 FDA reports)
GALLBLADDER DISORDER ( 273 FDA reports)
MALAISE ( 270 FDA reports)
OSTEONECROSIS OF JAW ( 270 FDA reports)
DECREASED APPETITE ( 266 FDA reports)
HYPOAESTHESIA ( 265 FDA reports)
ANHEDONIA ( 256 FDA reports)
RENAL FAILURE ( 255 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 254 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 251 FDA reports)
ATRIAL FIBRILLATION ( 246 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 245 FDA reports)
THROMBOCYTOPENIA ( 240 FDA reports)
SINUSITIS ( 226 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 225 FDA reports)
GAIT DISTURBANCE ( 225 FDA reports)
OSTEOARTHRITIS ( 222 FDA reports)
SEPSIS ( 220 FDA reports)
PRURITUS ( 219 FDA reports)
CONDITION AGGRAVATED ( 212 FDA reports)
BONE DISORDER ( 209 FDA reports)
HYPERSENSITIVITY ( 202 FDA reports)
TACHYCARDIA ( 200 FDA reports)
DYSPEPSIA ( 198 FDA reports)
MUSCULAR WEAKNESS ( 194 FDA reports)
DYSPHAGIA ( 191 FDA reports)
ECONOMIC PROBLEM ( 187 FDA reports)
DEATH ( 182 FDA reports)
NEUROPATHY PERIPHERAL ( 182 FDA reports)
PALPITATIONS ( 181 FDA reports)
PARAESTHESIA ( 180 FDA reports)
RESPIRATORY FAILURE ( 180 FDA reports)
SPINAL OSTEOARTHRITIS ( 177 FDA reports)
INFECTION ( 174 FDA reports)
SYNCOPE ( 170 FDA reports)
CONFUSIONAL STATE ( 169 FDA reports)
LOSS OF CONSCIOUSNESS ( 168 FDA reports)
PLEURAL EFFUSION ( 166 FDA reports)
MYALGIA ( 165 FDA reports)
BLOOD CREATININE INCREASED ( 162 FDA reports)
BLOOD PRESSURE INCREASED ( 161 FDA reports)
FEELING ABNORMAL ( 161 FDA reports)
MYOCARDIAL INFARCTION ( 159 FDA reports)
PAIN IN JAW ( 159 FDA reports)
CARDIAC ARREST ( 154 FDA reports)
TOOTH EXTRACTION ( 154 FDA reports)
WEIGHT INCREASED ( 154 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 153 FDA reports)
CHILLS ( 152 FDA reports)
IMPAIRED HEALING ( 152 FDA reports)
CEREBROVASCULAR ACCIDENT ( 151 FDA reports)
MENTAL DISORDER ( 149 FDA reports)
HYPERHIDROSIS ( 147 FDA reports)
CELLULITIS ( 146 FDA reports)
CONTUSION ( 146 FDA reports)
TREMOR ( 146 FDA reports)
ERYTHEMA ( 145 FDA reports)
DRUG HYPERSENSITIVITY ( 144 FDA reports)
MUSCLE SPASMS ( 143 FDA reports)
RENAL FAILURE CHRONIC ( 143 FDA reports)
HAEMOGLOBIN DECREASED ( 142 FDA reports)
HIATUS HERNIA ( 141 FDA reports)
OSTEOMYELITIS ( 138 FDA reports)
PANCYTOPENIA ( 138 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 137 FDA reports)
BLOOD GLUCOSE INCREASED ( 137 FDA reports)
HYPERLIPIDAEMIA ( 137 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 137 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 137 FDA reports)
MITRAL VALVE INCOMPETENCE ( 137 FDA reports)
URTICARIA ( 134 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 133 FDA reports)
PANCREATITIS ( 132 FDA reports)
BONE LESION ( 130 FDA reports)
ASTHMA ( 129 FDA reports)
CHEST DISCOMFORT ( 129 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 129 FDA reports)
ATELECTASIS ( 128 FDA reports)
CONVULSION ( 127 FDA reports)
ABDOMINAL DISTENSION ( 124 FDA reports)
NASOPHARYNGITIS ( 124 FDA reports)
HYPOXIA ( 121 FDA reports)
MUSCULOSKELETAL PAIN ( 121 FDA reports)
SWELLING ( 119 FDA reports)
LYMPHADENOPATHY ( 118 FDA reports)
DIABETES MELLITUS ( 117 FDA reports)
GASTRITIS ( 117 FDA reports)
HAEMORRHOIDS ( 117 FDA reports)
HEART RATE INCREASED ( 117 FDA reports)
MENTAL STATUS CHANGES ( 117 FDA reports)
BONE PAIN ( 116 FDA reports)
BRADYCARDIA ( 116 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 116 FDA reports)
TOOTHACHE ( 116 FDA reports)
HYPONATRAEMIA ( 115 FDA reports)
OSTEONECROSIS ( 114 FDA reports)
HYPOKALAEMIA ( 113 FDA reports)
VISION BLURRED ( 113 FDA reports)
BILIARY DYSKINESIA ( 112 FDA reports)
EAR PAIN ( 112 FDA reports)
HAEMATURIA ( 112 FDA reports)
NECK PAIN ( 111 FDA reports)
OSTEOPOROSIS ( 111 FDA reports)
RESPIRATORY DISTRESS ( 111 FDA reports)
BALANCE DISORDER ( 109 FDA reports)
MULTIPLE INJURIES ( 109 FDA reports)
PULMONARY HYPERTENSION ( 109 FDA reports)
PRODUCTIVE COUGH ( 108 FDA reports)
SOMNOLENCE ( 108 FDA reports)
METASTASES TO BONE ( 106 FDA reports)
VISUAL IMPAIRMENT ( 106 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 105 FDA reports)
SUICIDAL IDEATION ( 105 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 104 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 103 FDA reports)
DISABILITY ( 103 FDA reports)
RHABDOMYOLYSIS ( 103 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 103 FDA reports)
CARDIOMEGALY ( 102 FDA reports)
MULTI-ORGAN FAILURE ( 102 FDA reports)
NEUTROPENIA ( 101 FDA reports)
THROMBOSIS ( 101 FDA reports)
RENAL IMPAIRMENT ( 100 FDA reports)
WHEEZING ( 100 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 99 FDA reports)
PULMONARY OEDEMA ( 99 FDA reports)
RECTAL HAEMORRHAGE ( 99 FDA reports)
DEAFNESS ( 98 FDA reports)
DEFORMITY ( 97 FDA reports)
SWELLING FACE ( 97 FDA reports)
AMNESIA ( 96 FDA reports)
DYSPNOEA EXERTIONAL ( 96 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 96 FDA reports)
POLLAKIURIA ( 96 FDA reports)
ARTHRITIS ( 95 FDA reports)
CORONARY ARTERY DISEASE ( 95 FDA reports)
OEDEMA ( 95 FDA reports)
SLEEP DISORDER ( 95 FDA reports)
LUNG INFILTRATION ( 94 FDA reports)
SINUS TACHYCARDIA ( 94 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 94 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 93 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 92 FDA reports)
NEOPLASM MALIGNANT ( 92 FDA reports)
SLEEP APNOEA SYNDROME ( 92 FDA reports)
SCAR ( 91 FDA reports)
STAPHYLOCOCCAL INFECTION ( 91 FDA reports)
PLATELET COUNT DECREASED ( 90 FDA reports)
TINNITUS ( 90 FDA reports)
EXOSTOSIS ( 89 FDA reports)
ABDOMINAL DISCOMFORT ( 88 FDA reports)
LUNG NEOPLASM ( 88 FDA reports)
AGITATION ( 87 FDA reports)
ARRHYTHMIA ( 87 FDA reports)
DECREASED INTEREST ( 87 FDA reports)
FEBRILE NEUTROPENIA ( 87 FDA reports)
LEUKOPENIA ( 87 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 87 FDA reports)
HAEMOPTYSIS ( 86 FDA reports)
STRESS ( 86 FDA reports)
CARDIAC FAILURE ( 85 FDA reports)
HALLUCINATION ( 85 FDA reports)
ORAL DISORDER ( 85 FDA reports)
UNEVALUABLE EVENT ( 85 FDA reports)
AGGRESSION ( 84 FDA reports)
CARDIOMYOPATHY ( 84 FDA reports)
OROPHARYNGEAL PAIN ( 84 FDA reports)
TOOTH ABSCESS ( 84 FDA reports)
ALOPECIA ( 83 FDA reports)
EATING DISORDER ( 83 FDA reports)
HAEMATOCRIT DECREASED ( 83 FDA reports)
MIGRAINE ( 83 FDA reports)
LETHARGY ( 82 FDA reports)
DISCOMFORT ( 81 FDA reports)
FEAR ( 81 FDA reports)
JAUNDICE ( 81 FDA reports)
OSTEOPENIA ( 81 FDA reports)
STEVENS-JOHNSON SYNDROME ( 81 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 80 FDA reports)
LUNG DISORDER ( 80 FDA reports)
DYSGEUSIA ( 79 FDA reports)
TOOTH LOSS ( 79 FDA reports)
ENDODONTIC PROCEDURE ( 78 FDA reports)
HYPOTHYROIDISM ( 78 FDA reports)
ROTATOR CUFF SYNDROME ( 78 FDA reports)
CHOLECYSTITIS ( 77 FDA reports)
MEMORY IMPAIRMENT ( 76 FDA reports)
PERICARDIAL EFFUSION ( 76 FDA reports)
CARDIAC DISORDER ( 75 FDA reports)
CARDIAC MURMUR ( 75 FDA reports)
CARDIO-RESPIRATORY ARREST ( 75 FDA reports)
RHINITIS ALLERGIC ( 75 FDA reports)
HEART RATE IRREGULAR ( 74 FDA reports)
METASTASES TO LIVER ( 74 FDA reports)
ROAD TRAFFIC ACCIDENT ( 74 FDA reports)
ANGINA PECTORIS ( 73 FDA reports)
HERPES ZOSTER ( 73 FDA reports)
PHYSICAL DISABILITY ( 72 FDA reports)
RENAL CYST ( 72 FDA reports)
SURGERY ( 72 FDA reports)
DISEASE PROGRESSION ( 71 FDA reports)
LEUKOCYTOSIS ( 71 FDA reports)
NEPHROLITHIASIS ( 71 FDA reports)
SPEECH DISORDER ( 71 FDA reports)
VENTRICULAR TACHYCARDIA ( 71 FDA reports)
INFLAMMATION ( 70 FDA reports)
ILL-DEFINED DISORDER ( 69 FDA reports)
MULTIPLE MYELOMA ( 69 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 69 FDA reports)
EJECTION FRACTION DECREASED ( 68 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 68 FDA reports)
EMOTIONAL DISORDER ( 67 FDA reports)
HAEMORRHAGE ( 67 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 67 FDA reports)
ORAL CANDIDIASIS ( 67 FDA reports)
HAEMATOCHEZIA ( 66 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 66 FDA reports)
SCOLIOSIS ( 66 FDA reports)
GASTROINTESTINAL DISORDER ( 65 FDA reports)
JOINT SWELLING ( 65 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 65 FDA reports)
BLOOD UREA INCREASED ( 64 FDA reports)
BURSITIS ( 64 FDA reports)
DYSURIA ( 64 FDA reports)
HYPERCHOLESTEROLAEMIA ( 64 FDA reports)
PULMONARY CONGESTION ( 64 FDA reports)
EPISTAXIS ( 63 FDA reports)
HEPATIC STEATOSIS ( 63 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 62 FDA reports)
CHOLECYSTITIS ACUTE ( 62 FDA reports)
DYSKINESIA ( 62 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 61 FDA reports)
ACUTE RESPIRATORY FAILURE ( 61 FDA reports)
DYSARTHRIA ( 61 FDA reports)
HEPATIC ENZYME INCREASED ( 61 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 60 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 60 FDA reports)
EYE PAIN ( 60 FDA reports)
HEPATITIS ( 60 FDA reports)
NIGHT SWEATS ( 60 FDA reports)
ORTHOSTATIC HYPOTENSION ( 60 FDA reports)
PULMONARY INFARCTION ( 60 FDA reports)
ARTHROPATHY ( 59 FDA reports)
BILIARY COLIC ( 59 FDA reports)
CYANOSIS ( 59 FDA reports)
DISTURBANCE IN ATTENTION ( 59 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 59 FDA reports)
LIVER DISORDER ( 59 FDA reports)
SEPTIC SHOCK ( 59 FDA reports)
VENTRICULAR FIBRILLATION ( 59 FDA reports)
SPINAL COMPRESSION FRACTURE ( 58 FDA reports)
ANGER ( 57 FDA reports)
ARTERIOSCLEROSIS ( 57 FDA reports)
CANDIDIASIS ( 57 FDA reports)
DENTAL CARIES ( 57 FDA reports)
EMPHYSEMA ( 57 FDA reports)
PNEUMOTHORAX ( 57 FDA reports)
PRODUCT QUALITY ISSUE ( 57 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 57 FDA reports)
DYSLIPIDAEMIA ( 56 FDA reports)
HYPERGLYCAEMIA ( 56 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 56 FDA reports)
SUICIDE ATTEMPT ( 56 FDA reports)
ABNORMAL BEHAVIOUR ( 55 FDA reports)
GLAUCOMA ( 55 FDA reports)
MOBILITY DECREASED ( 55 FDA reports)
RIB FRACTURE ( 55 FDA reports)
VERTIGO ( 55 FDA reports)
BLOOD BILIRUBIN INCREASED ( 54 FDA reports)
DRY MOUTH ( 54 FDA reports)
FOOT FRACTURE ( 54 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 54 FDA reports)
NERVOUSNESS ( 54 FDA reports)
RESPIRATORY TRACT INFECTION ( 54 FDA reports)
TREATMENT NONCOMPLIANCE ( 54 FDA reports)
BURNING SENSATION ( 53 FDA reports)
COGNITIVE DISORDER ( 53 FDA reports)
HYPOPHAGIA ( 53 FDA reports)
IRRITABILITY ( 53 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 53 FDA reports)
SYNOVIAL CYST ( 53 FDA reports)
DIVERTICULUM ( 52 FDA reports)
EAR INFECTION ( 52 FDA reports)
JOINT INJURY ( 52 FDA reports)
OBESITY ( 52 FDA reports)
PANIC ATTACK ( 52 FDA reports)
PROTHROMBIN TIME PROLONGED ( 52 FDA reports)
SKIN DISCOLOURATION ( 52 FDA reports)
TYPE 2 DIABETES MELLITUS ( 52 FDA reports)
URINARY INCONTINENCE ( 52 FDA reports)
BLISTER ( 51 FDA reports)
CHOLECYSTECTOMY ( 51 FDA reports)
DISORIENTATION ( 51 FDA reports)
HYPOGLYCAEMIA ( 51 FDA reports)
PATHOLOGICAL FRACTURE ( 51 FDA reports)
RASH MACULO-PAPULAR ( 51 FDA reports)
SKIN LESION ( 51 FDA reports)
SKIN ULCER ( 51 FDA reports)
HEPATOTOXICITY ( 50 FDA reports)
INFLUENZA ( 50 FDA reports)
LIP SWELLING ( 50 FDA reports)
ORAL PAIN ( 50 FDA reports)
RASH PRURITIC ( 50 FDA reports)
TARDIVE DYSKINESIA ( 50 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 50 FDA reports)
BASAL CELL CARCINOMA ( 49 FDA reports)
COLITIS ( 49 FDA reports)
HAEMATOMA ( 49 FDA reports)
INFLUENZA LIKE ILLNESS ( 49 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 49 FDA reports)
STOMATITIS ( 49 FDA reports)
ATAXIA ( 48 FDA reports)
BLOOD PRESSURE DECREASED ( 48 FDA reports)
DELIRIUM ( 48 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 48 FDA reports)
DRUG ERUPTION ( 48 FDA reports)
FLUID OVERLOAD ( 48 FDA reports)
GALLBLADDER INJURY ( 48 FDA reports)
HYPERCALCAEMIA ( 48 FDA reports)
INCORRECT DOSE ADMINISTERED ( 48 FDA reports)
OSTEITIS ( 48 FDA reports)
RASH GENERALISED ( 48 FDA reports)
SKIN EXFOLIATION ( 48 FDA reports)
TORSADE DE POINTES ( 48 FDA reports)
ANAPHYLACTIC REACTION ( 47 FDA reports)
CATARACT ( 47 FDA reports)
ECZEMA ( 47 FDA reports)
GINGIVAL PAIN ( 47 FDA reports)
MEDICATION ERROR ( 47 FDA reports)
ORAL CAVITY FISTULA ( 47 FDA reports)
PALLOR ( 47 FDA reports)
TENDONITIS ( 47 FDA reports)
ABDOMINAL TENDERNESS ( 46 FDA reports)
CEREBRAL ATROPHY ( 46 FDA reports)
FLATULENCE ( 46 FDA reports)
HYPERKALAEMIA ( 46 FDA reports)
IRRITABLE BOWEL SYNDROME ( 46 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 46 FDA reports)
NASAL CONGESTION ( 46 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 46 FDA reports)
PHARYNGITIS ( 46 FDA reports)
RESPIRATORY DISORDER ( 46 FDA reports)
VISUAL ACUITY REDUCED ( 46 FDA reports)
ABASIA ( 45 FDA reports)
CEREBRAL INFARCTION ( 45 FDA reports)
ERECTILE DYSFUNCTION ( 45 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 45 FDA reports)
LIMB INJURY ( 45 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 45 FDA reports)
OSTEOLYSIS ( 45 FDA reports)
PROCTALGIA ( 45 FDA reports)
URINARY RETENTION ( 45 FDA reports)
VIRAL INFECTION ( 45 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 44 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 44 FDA reports)
CHRONIC SINUSITIS ( 44 FDA reports)
COAGULOPATHY ( 44 FDA reports)
HEPATIC FAILURE ( 44 FDA reports)
HERPES SIMPLEX ( 44 FDA reports)
HOT FLUSH ( 44 FDA reports)
SEBORRHOEIC KERATOSIS ( 44 FDA reports)
SPINAL COLUMN STENOSIS ( 44 FDA reports)
AGEUSIA ( 43 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 43 FDA reports)
CARDIOGENIC SHOCK ( 43 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 43 FDA reports)
GASTROENTERITIS ( 43 FDA reports)
HYPOACUSIS ( 43 FDA reports)
SWOLLEN TONGUE ( 43 FDA reports)
COLITIS ISCHAEMIC ( 42 FDA reports)
DEPRESSED MOOD ( 42 FDA reports)
DYSPHONIA ( 42 FDA reports)
ENCEPHALOPATHY ( 42 FDA reports)
FAECAL INCONTINENCE ( 42 FDA reports)
FIBROMYALGIA ( 42 FDA reports)
FLUSHING ( 42 FDA reports)
GASTRIC ULCER ( 42 FDA reports)
LOOSE TOOTH ( 42 FDA reports)
ODYNOPHAGIA ( 42 FDA reports)
OXYGEN SATURATION DECREASED ( 42 FDA reports)
RHINORRHOEA ( 42 FDA reports)
STRESS FRACTURE ( 42 FDA reports)
TACHYPNOEA ( 42 FDA reports)
UNRESPONSIVE TO STIMULI ( 42 FDA reports)
BREATH SOUNDS ABNORMAL ( 41 FDA reports)
DRUG TOXICITY ( 41 FDA reports)
LUMBAR RADICULOPATHY ( 41 FDA reports)
MICTURITION URGENCY ( 41 FDA reports)
MUCOSAL INFLAMMATION ( 41 FDA reports)
PNEUMONIA ASPIRATION ( 41 FDA reports)
PRESYNCOPE ( 41 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 41 FDA reports)
RESPIRATORY ARREST ( 41 FDA reports)
MASS ( 40 FDA reports)
METABOLIC ACIDOSIS ( 40 FDA reports)
TOOTH DISORDER ( 40 FDA reports)
BLOOD POTASSIUM INCREASED ( 39 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 39 FDA reports)
OFF LABEL USE ( 39 FDA reports)
QUALITY OF LIFE DECREASED ( 39 FDA reports)
RENAL DISORDER ( 39 FDA reports)
SPONDYLOLISTHESIS ( 39 FDA reports)
TENDON RUPTURE ( 39 FDA reports)
ACUTE CORONARY SYNDROME ( 38 FDA reports)
APHASIA ( 38 FDA reports)
BLOOD SODIUM DECREASED ( 38 FDA reports)
CAROTID ARTERY STENOSIS ( 38 FDA reports)
COMA ( 38 FDA reports)
CONJUNCTIVITIS ( 38 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 38 FDA reports)
GOUT ( 38 FDA reports)
NEURALGIA ( 38 FDA reports)
OVERDOSE ( 38 FDA reports)
REFLUX OESOPHAGITIS ( 38 FDA reports)
ASCITES ( 37 FDA reports)
BODY TEMPERATURE INCREASED ( 37 FDA reports)
DIVERTICULITIS ( 37 FDA reports)
FEMUR FRACTURE ( 37 FDA reports)
GINGIVAL DISORDER ( 37 FDA reports)
METASTASES TO SPINE ( 37 FDA reports)
ORAL INFECTION ( 37 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 36 FDA reports)
DRUG INTOLERANCE ( 36 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 36 FDA reports)
INGROWING NAIL ( 36 FDA reports)
PELVIC PAIN ( 36 FDA reports)
PSYCHOTIC DISORDER ( 36 FDA reports)
PULMONARY FIBROSIS ( 36 FDA reports)
PURULENT DISCHARGE ( 36 FDA reports)
RALES ( 36 FDA reports)
RESTLESS LEGS SYNDROME ( 36 FDA reports)
TOOTH FRACTURE ( 36 FDA reports)
ABORTION SPONTANEOUS ( 35 FDA reports)
ANKLE FRACTURE ( 35 FDA reports)
ANOSMIA ( 35 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 35 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 35 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 35 FDA reports)
CIRCULATORY COLLAPSE ( 35 FDA reports)
DILATATION VENTRICULAR ( 35 FDA reports)
LYMPHOMA ( 35 FDA reports)
ORAL INTAKE REDUCED ( 35 FDA reports)
PHARYNGEAL OEDEMA ( 35 FDA reports)
SINUS DISORDER ( 35 FDA reports)
SPUTUM DISCOLOURED ( 35 FDA reports)
TOOTH INFECTION ( 35 FDA reports)
ANOREXIA ( 34 FDA reports)
AORTIC VALVE INCOMPETENCE ( 34 FDA reports)
ATRIAL SEPTAL DEFECT ( 34 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 34 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 34 FDA reports)
HIP FRACTURE ( 34 FDA reports)
JOINT EFFUSION ( 34 FDA reports)
LYMPHOEDEMA ( 34 FDA reports)
MUSCLE TIGHTNESS ( 34 FDA reports)
NERVOUS SYSTEM DISORDER ( 34 FDA reports)
OTITIS MEDIA ( 34 FDA reports)
PERIPHERAL COLDNESS ( 34 FDA reports)
PROCEDURAL PAIN ( 34 FDA reports)
PSEUDOMONAS INFECTION ( 34 FDA reports)
RESTLESSNESS ( 34 FDA reports)
SUBDURAL HAEMATOMA ( 34 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 34 FDA reports)
AREFLEXIA ( 33 FDA reports)
BONE MARROW FAILURE ( 33 FDA reports)
CHROMATURIA ( 33 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 33 FDA reports)
DRUG LEVEL INCREASED ( 33 FDA reports)
FEELING HOT ( 33 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 33 FDA reports)
HYPOAESTHESIA ORAL ( 33 FDA reports)
IMPAIRED WORK ABILITY ( 33 FDA reports)
INTERSTITIAL LUNG DISEASE ( 33 FDA reports)
LACERATION ( 33 FDA reports)
LUNG INFECTION ( 33 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 33 FDA reports)
RENAL TUBULAR NECROSIS ( 33 FDA reports)
SNORING ( 33 FDA reports)
ABSCESS DRAINAGE ( 32 FDA reports)
ACTINIC KERATOSIS ( 32 FDA reports)
ADRENAL INSUFFICIENCY ( 32 FDA reports)
BREAST CANCER ( 32 FDA reports)
COMPRESSION FRACTURE ( 32 FDA reports)
DIALYSIS ( 32 FDA reports)
DISEASE RECURRENCE ( 32 FDA reports)
HEMIPARESIS ( 32 FDA reports)
HEPATIC CYST ( 32 FDA reports)
HEPATOMEGALY ( 32 FDA reports)
KYPHOSIS ( 32 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 32 FDA reports)
MENISCUS LESION ( 32 FDA reports)
MITRAL VALVE PROLAPSE ( 32 FDA reports)
MOOD SWINGS ( 32 FDA reports)
NEOPLASM PROGRESSION ( 32 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 32 FDA reports)
OVARIAN CYST ( 32 FDA reports)
SEROMA ( 32 FDA reports)
THROAT IRRITATION ( 32 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 32 FDA reports)
BIPOLAR DISORDER ( 31 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 31 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 31 FDA reports)
EXPOSED BONE IN JAW ( 31 FDA reports)
HEART RATE DECREASED ( 31 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 31 FDA reports)
MALNUTRITION ( 31 FDA reports)
SHOCK ( 31 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 31 FDA reports)
BLOOD POTASSIUM DECREASED ( 30 FDA reports)
CEREBRAL HAEMORRHAGE ( 30 FDA reports)
COLONIC POLYP ( 30 FDA reports)
DEVICE RELATED INFECTION ( 30 FDA reports)
EOSINOPHILIA ( 30 FDA reports)
LACTIC ACIDOSIS ( 30 FDA reports)
MOVEMENT DISORDER ( 30 FDA reports)
NOCTURIA ( 30 FDA reports)
ONYCHOMYCOSIS ( 30 FDA reports)
SPLENOMEGALY ( 30 FDA reports)
ANGIOEDEMA ( 29 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 29 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 29 FDA reports)
BRONCHIECTASIS ( 29 FDA reports)
CERVICAL SPINAL STENOSIS ( 29 FDA reports)
CRYING ( 29 FDA reports)
GASTROENTERITIS VIRAL ( 29 FDA reports)
HAEMOLYTIC ANAEMIA ( 29 FDA reports)
HYPERKERATOSIS ( 29 FDA reports)
INTENTIONAL OVERDOSE ( 29 FDA reports)
LEFT ATRIAL DILATATION ( 29 FDA reports)
LOBAR PNEUMONIA ( 29 FDA reports)
MYOCARDIAL ISCHAEMIA ( 29 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 29 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 29 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 29 FDA reports)
THROAT TIGHTNESS ( 29 FDA reports)
ABDOMINAL PAIN LOWER ( 28 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 28 FDA reports)
BRUXISM ( 28 FDA reports)
CARDIOVASCULAR DISORDER ( 28 FDA reports)
DUODENITIS ( 28 FDA reports)
HAEMATEMESIS ( 28 FDA reports)
ILEUS ( 28 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 28 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 28 FDA reports)
JOINT SPRAIN ( 28 FDA reports)
MAJOR DEPRESSION ( 28 FDA reports)
MOUTH HAEMORRHAGE ( 28 FDA reports)
PANCREATITIS ACUTE ( 28 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 28 FDA reports)
PLEURISY ( 28 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 28 FDA reports)
WALKING DISABILITY ( 28 FDA reports)
ACIDOSIS ( 27 FDA reports)
ACNE ( 27 FDA reports)
APNOEA ( 27 FDA reports)
BONE DEBRIDEMENT ( 27 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 27 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 27 FDA reports)
DUODENAL ULCER ( 27 FDA reports)
EOSINOPHIL COUNT INCREASED ( 27 FDA reports)
FIBULA FRACTURE ( 27 FDA reports)
FLUID RETENTION ( 27 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 27 FDA reports)
LIGAMENT RUPTURE ( 27 FDA reports)
ORTHOPNOEA ( 27 FDA reports)
PERIPHERAL ISCHAEMIA ( 27 FDA reports)
PSORIASIS ( 27 FDA reports)
SUBCUTANEOUS ABSCESS ( 27 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 27 FDA reports)
VISUAL FIELD DEFECT ( 27 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 27 FDA reports)
ABSCESS ( 26 FDA reports)
CYST ( 26 FDA reports)
DRY EYE ( 26 FDA reports)
ECCHYMOSIS ( 26 FDA reports)
FACE OEDEMA ( 26 FDA reports)
FEELING COLD ( 26 FDA reports)
FLANK PAIN ( 26 FDA reports)
FUNGAL INFECTION ( 26 FDA reports)
GRAND MAL CONVULSION ( 26 FDA reports)
HUMERUS FRACTURE ( 26 FDA reports)
HYDRONEPHROSIS ( 26 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 26 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 26 FDA reports)
METASTASES TO THORAX ( 26 FDA reports)
PAROSMIA ( 26 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 26 FDA reports)
PREGNANCY ( 26 FDA reports)
PREMATURE BABY ( 26 FDA reports)
PRURITUS GENERALISED ( 26 FDA reports)
RASH ERYTHEMATOUS ( 26 FDA reports)
THYROID DISORDER ( 26 FDA reports)
UVEITIS ( 26 FDA reports)
VAGINAL HAEMORRHAGE ( 26 FDA reports)
BACTERIAL INFECTION ( 25 FDA reports)
CERUMEN IMPACTION ( 25 FDA reports)
EAR CONGESTION ( 25 FDA reports)
FACE INJURY ( 25 FDA reports)
HAEMANGIOMA ( 25 FDA reports)
HYPERBILIRUBINAEMIA ( 25 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 25 FDA reports)
INFUSION RELATED REACTION ( 25 FDA reports)
INTENTIONAL DRUG MISUSE ( 25 FDA reports)
IRON DEFICIENCY ANAEMIA ( 25 FDA reports)
JAW OPERATION ( 25 FDA reports)
MUSCLE TWITCHING ( 25 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 25 FDA reports)
OESOPHAGITIS ( 25 FDA reports)
OSTEOSCLEROSIS ( 25 FDA reports)
PNEUMONITIS ( 25 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 25 FDA reports)
RADIOTHERAPY ( 25 FDA reports)
SECONDARY SEQUESTRUM ( 25 FDA reports)
SINUS BRADYCARDIA ( 25 FDA reports)
SINUS CONGESTION ( 25 FDA reports)
ABNORMAL DREAMS ( 24 FDA reports)
ACTINOMYCOSIS ( 24 FDA reports)
ANGINA UNSTABLE ( 24 FDA reports)
ATRIAL FLUTTER ( 24 FDA reports)
AZOTAEMIA ( 24 FDA reports)
CEREBRAL ISCHAEMIA ( 24 FDA reports)
DIABETIC NEUROPATHY ( 24 FDA reports)
DIPLOPIA ( 24 FDA reports)
EXCORIATION ( 24 FDA reports)
EYE DISORDER ( 24 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 24 FDA reports)
INTESTINAL OBSTRUCTION ( 24 FDA reports)
LICHENOID KERATOSIS ( 24 FDA reports)
LIMB DISCOMFORT ( 24 FDA reports)
LOCAL SWELLING ( 24 FDA reports)
LUMBAR SPINAL STENOSIS ( 24 FDA reports)
NIGHTMARE ( 24 FDA reports)
PLANTAR FASCIITIS ( 24 FDA reports)
POSTURE ABNORMAL ( 24 FDA reports)
PULSE ABSENT ( 24 FDA reports)
SPINAL LAMINECTOMY ( 24 FDA reports)
ADRENAL NEOPLASM ( 23 FDA reports)
AORTIC ANEURYSM ( 23 FDA reports)
BRONCHOSPASM ( 23 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 23 FDA reports)
DEBRIDEMENT ( 23 FDA reports)
DERMAL CYST ( 23 FDA reports)
ERYTHEMA MULTIFORME ( 23 FDA reports)
FOOT DEFORMITY ( 23 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 23 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 23 FDA reports)
HALLUCINATION, VISUAL ( 23 FDA reports)
HEPATIC LESION ( 23 FDA reports)
HYPERCOAGULATION ( 23 FDA reports)
LIPOMA ( 23 FDA reports)
LIVER INJURY ( 23 FDA reports)
MUSCLE STRAIN ( 23 FDA reports)
MYELODYSPLASTIC SYNDROME ( 23 FDA reports)
OSTEOMYELITIS CHRONIC ( 23 FDA reports)
PATHOGEN RESISTANCE ( 23 FDA reports)
POLYP ( 23 FDA reports)
SPINAL FRACTURE ( 23 FDA reports)
SUDDEN DEATH ( 23 FDA reports)
THIRST ( 23 FDA reports)
WOUND DEHISCENCE ( 23 FDA reports)
BREATH ODOUR ( 22 FDA reports)
CLOSTRIDIAL INFECTION ( 22 FDA reports)
CYSTITIS ( 22 FDA reports)
DYSTONIA ( 22 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 22 FDA reports)
HEPATITIS ACUTE ( 22 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 22 FDA reports)
HYPERTONIC BLADDER ( 22 FDA reports)
INCOHERENT ( 22 FDA reports)
ISCHAEMIA ( 22 FDA reports)
LACRIMATION INCREASED ( 22 FDA reports)
LIGAMENT SPRAIN ( 22 FDA reports)
MASTICATION DISORDER ( 22 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 22 FDA reports)
PHLEBITIS ( 22 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 22 FDA reports)
RASH PUSTULAR ( 22 FDA reports)
RECTOCELE ( 22 FDA reports)
RHINITIS ( 22 FDA reports)
RHONCHI ( 22 FDA reports)
THERAPY NON-RESPONDER ( 22 FDA reports)
TUBERCULOSIS ( 22 FDA reports)
UMBILICAL HERNIA ( 22 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
ADVERSE EVENT ( 21 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
BLOOD CALCIUM DECREASED ( 21 FDA reports)
CARPAL TUNNEL SYNDROME ( 21 FDA reports)
CHOLESTEROSIS ( 21 FDA reports)
CYSTOCELE ( 21 FDA reports)
DECUBITUS ULCER ( 21 FDA reports)
DRUG DOSE OMISSION ( 21 FDA reports)
DYSSTASIA ( 21 FDA reports)
ERUCTATION ( 21 FDA reports)
GASTRIC DISORDER ( 21 FDA reports)
HALLUCINATION, AUDITORY ( 21 FDA reports)
HEAD INJURY ( 21 FDA reports)
HYPOCALCAEMIA ( 21 FDA reports)
KAPOSI'S SARCOMA ( 21 FDA reports)
LUNG CONSOLIDATION ( 21 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 21 FDA reports)
PLEURITIC PAIN ( 21 FDA reports)
RASH PAPULAR ( 21 FDA reports)
RETCHING ( 21 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 21 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 21 FDA reports)
TENDERNESS ( 21 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 21 FDA reports)
VASCULAR ANOMALY ( 21 FDA reports)
ANOGENITAL WARTS ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
BLOOD URINE PRESENT ( 20 FDA reports)
BODY HEIGHT DECREASED ( 20 FDA reports)
CARDIAC VALVE DISEASE ( 20 FDA reports)
DEAFNESS NEUROSENSORY ( 20 FDA reports)
DELUSION ( 20 FDA reports)
DENTAL OPERATION ( 20 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 20 FDA reports)
DRY SKIN ( 20 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 20 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 20 FDA reports)
EYE SWELLING ( 20 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 20 FDA reports)
FISTULA ( 20 FDA reports)
FRACTURE ( 20 FDA reports)
HAEMODIALYSIS ( 20 FDA reports)
HERPES VIRUS INFECTION ( 20 FDA reports)
HYPOTONIA ( 20 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 20 FDA reports)
IRON DEFICIENCY ( 20 FDA reports)
ISCHAEMIC STROKE ( 20 FDA reports)
LIPASE INCREASED ( 20 FDA reports)
LUNG HYPERINFLATION ( 20 FDA reports)
MELAENA ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MUSCLE ATROPHY ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
PARANOIA ( 20 FDA reports)
PROTEINURIA ( 20 FDA reports)
PULMONARY GRANULOMA ( 20 FDA reports)
PULMONARY MASS ( 20 FDA reports)
SKIN PAPILLOMA ( 20 FDA reports)
UTERINE HAEMORRHAGE ( 20 FDA reports)
VARICOSE VEIN ( 20 FDA reports)
ADVERSE DRUG REACTION ( 19 FDA reports)
ANURIA ( 19 FDA reports)
APHTHOUS STOMATITIS ( 19 FDA reports)
BACTERAEMIA ( 19 FDA reports)
DERMATITIS ( 19 FDA reports)
DRUG DEPENDENCE ( 19 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 19 FDA reports)
EPIGASTRIC DISCOMFORT ( 19 FDA reports)
EXERCISE TOLERANCE DECREASED ( 19 FDA reports)
GENERALISED OEDEMA ( 19 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 19 FDA reports)
HYPERSOMNIA ( 19 FDA reports)
INTERMITTENT CLAUDICATION ( 19 FDA reports)
INTESTINAL PERFORATION ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
MAMMOGRAM ABNORMAL ( 19 FDA reports)
NODULE ( 19 FDA reports)
PEPTIC ULCER ( 19 FDA reports)
PETECHIAE ( 19 FDA reports)
PHOTOPSIA ( 19 FDA reports)
PLASMACYTOMA ( 19 FDA reports)
PULMONARY VALVE STENOSIS ( 19 FDA reports)
RECTAL ABSCESS ( 19 FDA reports)
RECTAL FISSURE ( 19 FDA reports)
RENAL INJURY ( 19 FDA reports)
SCIATICA ( 19 FDA reports)
SKIN TIGHTNESS ( 19 FDA reports)
SOMNAMBULISM ( 19 FDA reports)
TOOTH IMPACTED ( 19 FDA reports)
TRIGEMINAL NEURALGIA ( 19 FDA reports)
WOUND ( 19 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 18 FDA reports)
BLOOD ALBUMIN DECREASED ( 18 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 18 FDA reports)
CHEST X-RAY ABNORMAL ( 18 FDA reports)
COLD SWEAT ( 18 FDA reports)
CYTOLYTIC HEPATITIS ( 18 FDA reports)
DEMENTIA ( 18 FDA reports)
EYE PRURITUS ( 18 FDA reports)
FAECES DISCOLOURED ( 18 FDA reports)
GASTRIC POLYPS ( 18 FDA reports)
HAEMOLYSIS ( 18 FDA reports)
HEARING IMPAIRED ( 18 FDA reports)
HEPATIC CIRRHOSIS ( 18 FDA reports)
HEPATIC MASS ( 18 FDA reports)
METASTATIC NEOPLASM ( 18 FDA reports)
MULTIPLE ALLERGIES ( 18 FDA reports)
MUSCLE INJURY ( 18 FDA reports)
MYOSITIS ( 18 FDA reports)
NEPHROSCLEROSIS ( 18 FDA reports)
NEUTROPHIL COUNT DECREASED ( 18 FDA reports)
ORAL DISCOMFORT ( 18 FDA reports)
PARKINSONISM ( 18 FDA reports)
PERIODONTITIS ( 18 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 18 FDA reports)
RESPIRATORY RATE INCREASED ( 18 FDA reports)
SENSORY DISTURBANCE ( 18 FDA reports)
SEQUESTRECTOMY ( 18 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 18 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 18 FDA reports)
THROMBOPHLEBITIS ( 18 FDA reports)
TREATMENT FAILURE ( 18 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
VITREOUS FLOATERS ( 18 FDA reports)
AORTIC STENOSIS ( 17 FDA reports)
BLOOD CALCIUM INCREASED ( 17 FDA reports)
BLOOD CULTURE POSITIVE ( 17 FDA reports)
BLOOD URIC ACID INCREASED ( 17 FDA reports)
BONE EROSION ( 17 FDA reports)
CACHEXIA ( 17 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 17 FDA reports)
CEREBRAL THROMBOSIS ( 17 FDA reports)
CHOLESTASIS ( 17 FDA reports)
DECREASED ACTIVITY ( 17 FDA reports)
DENTAL CARE ( 17 FDA reports)
DERMATITIS ALLERGIC ( 17 FDA reports)
ENTEROCOCCAL INFECTION ( 17 FDA reports)
EXANTHEM ( 17 FDA reports)
FURUNCLE ( 17 FDA reports)
GOITRE ( 17 FDA reports)
HAEMATOCRIT INCREASED ( 17 FDA reports)
HERNIA ( 17 FDA reports)
HYPERREFLEXIA ( 17 FDA reports)
INCONTINENCE ( 17 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 17 FDA reports)
JAW FRACTURE ( 17 FDA reports)
MALIGNANT MELANOMA ( 17 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 17 FDA reports)
METASTASES TO LUNG ( 17 FDA reports)
PURPURA ( 17 FDA reports)
PURULENCE ( 17 FDA reports)
PYELONEPHRITIS ( 17 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 17 FDA reports)
SENSITIVITY OF TEETH ( 17 FDA reports)
SPUTUM CULTURE POSITIVE ( 17 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 17 FDA reports)
VULVOVAGINAL DRYNESS ( 17 FDA reports)
ABSCESS ORAL ( 16 FDA reports)
AMENORRHOEA ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
APHAGIA ( 16 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 16 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 16 FDA reports)
BREAST RECONSTRUCTION ( 16 FDA reports)
CARDIAC ANEURYSM ( 16 FDA reports)
CERVICAL DYSPLASIA ( 16 FDA reports)
CORONARY ARTERY STENOSIS ( 16 FDA reports)
DENTAL IMPLANTATION ( 16 FDA reports)
DIABETIC GASTROPARESIS ( 16 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 16 FDA reports)
GINGIVAL INFECTION ( 16 FDA reports)
GINGIVITIS ( 16 FDA reports)
HEART INJURY ( 16 FDA reports)
HEART SOUNDS ABNORMAL ( 16 FDA reports)
HEPATIC NECROSIS ( 16 FDA reports)
HYPOAESTHESIA FACIAL ( 16 FDA reports)
INTRACARDIAC THROMBUS ( 16 FDA reports)
LIBIDO DECREASED ( 16 FDA reports)
LYMPHOPENIA ( 16 FDA reports)
MOOD ALTERED ( 16 FDA reports)
NO THERAPEUTIC RESPONSE ( 16 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
ORAL HERPES ( 16 FDA reports)
OVERWEIGHT ( 16 FDA reports)
PARKINSON'S DISEASE ( 16 FDA reports)
PERIODONTAL DISEASE ( 16 FDA reports)
POLYARTHRITIS ( 16 FDA reports)
PROTEIN TOTAL INCREASED ( 16 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 16 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 16 FDA reports)
RHEUMATOID ARTHRITIS ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
SINUS HEADACHE ( 16 FDA reports)
UROSEPSIS ( 16 FDA reports)
WALKING AID USER ( 16 FDA reports)
ABDOMINAL MASS ( 15 FDA reports)
ACCIDENTAL OVERDOSE ( 15 FDA reports)
ADJUSTMENT DISORDER ( 15 FDA reports)
ANORECTAL DISCOMFORT ( 15 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 15 FDA reports)
B-CELL LYMPHOMA ( 15 FDA reports)
BLOOD CORTISOL ABNORMAL ( 15 FDA reports)
BONE NEOPLASM ( 15 FDA reports)
BRAIN OEDEMA ( 15 FDA reports)
CARDIAC PACEMAKER INSERTION ( 15 FDA reports)
COLLAPSE OF LUNG ( 15 FDA reports)
DIABETIC RETINOPATHY ( 15 FDA reports)
DRUG ADMINISTRATION ERROR ( 15 FDA reports)
DRUG SCREEN POSITIVE ( 15 FDA reports)
EYE IRRITATION ( 15 FDA reports)
EYELID OEDEMA ( 15 FDA reports)
GENITAL HERPES ( 15 FDA reports)
HOSPITALISATION ( 15 FDA reports)
HYPOMAGNESAEMIA ( 15 FDA reports)
HYPOVOLAEMIA ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 15 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
NASAL SEPTUM DEVIATION ( 15 FDA reports)
NERVE INJURY ( 15 FDA reports)
OSTEORADIONECROSIS ( 15 FDA reports)
PARAESTHESIA ORAL ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 15 FDA reports)
PROLAPSE REPAIR ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
PULPITIS DENTAL ( 15 FDA reports)
RADICULOPATHY ( 15 FDA reports)
RASH MACULAR ( 15 FDA reports)
SPINAL DISORDER ( 15 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 15 FDA reports)
TRANSAMINASES INCREASED ( 15 FDA reports)
VASCULAR PSEUDOANEURYSM ( 15 FDA reports)
VENTRICULAR HYPOKINESIA ( 15 FDA reports)
AKATHISIA ( 14 FDA reports)
ANGIOPATHY ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK ( 14 FDA reports)
AUTOIMMUNE HEPATITIS ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
BEDRIDDEN ( 14 FDA reports)
BLOOD AMYLASE INCREASED ( 14 FDA reports)
BLOOD DISORDER ( 14 FDA reports)
BONE FISTULA ( 14 FDA reports)
BONE SCAN ABNORMAL ( 14 FDA reports)
BRAIN MASS ( 14 FDA reports)
CAESAREAN SECTION ( 14 FDA reports)
CEREBROVASCULAR DISORDER ( 14 FDA reports)
CHLAMYDIAL INFECTION ( 14 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 14 FDA reports)
DRUG EFFECT DECREASED ( 14 FDA reports)
DRUG RESISTANCE ( 14 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 14 FDA reports)
FACIAL PAIN ( 14 FDA reports)
HAEMODYNAMIC INSTABILITY ( 14 FDA reports)
HYPERTENSIVE HEART DISEASE ( 14 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 14 FDA reports)
JOINT DISLOCATION ( 14 FDA reports)
JOINT STIFFNESS ( 14 FDA reports)
KNEE OPERATION ( 14 FDA reports)
LYMPHOCYTIC INFILTRATION ( 14 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 14 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
MELANOCYTIC NAEVUS ( 14 FDA reports)
MITRAL VALVE DISEASE ( 14 FDA reports)
MONOCYTOSIS ( 14 FDA reports)
MOUTH ULCERATION ( 14 FDA reports)
MYCOBACTERIAL INFECTION ( 14 FDA reports)
MYCOSIS FUNGOIDES ( 14 FDA reports)
NECK MASS ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
ORAL TORUS ( 14 FDA reports)
PERITONITIS ( 14 FDA reports)
POST PROCEDURAL COMPLICATION ( 14 FDA reports)
RADICULITIS ( 14 FDA reports)
SKIN EROSION ( 14 FDA reports)
SKIN INDURATION ( 14 FDA reports)
SPINAL CORD INJURY ( 14 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 14 FDA reports)
STILLBIRTH ( 14 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 14 FDA reports)
THYROID NEOPLASM ( 14 FDA reports)
TONGUE ULCERATION ( 14 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 14 FDA reports)
UTERINE LEIOMYOMA ( 14 FDA reports)
VAGINAL DISCHARGE ( 14 FDA reports)
VENTRICULAR ARRHYTHMIA ( 14 FDA reports)
VENTRICULAR HYPERTROPHY ( 14 FDA reports)
WHEELCHAIR USER ( 14 FDA reports)
X-RAY ABNORMAL ( 14 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 13 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 13 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 13 FDA reports)
BILE DUCT STONE ( 13 FDA reports)
BLINDNESS ( 13 FDA reports)
BLOOD CHLORIDE DECREASED ( 13 FDA reports)
BLOOD IRON INCREASED ( 13 FDA reports)
BONE DENSITY DECREASED ( 13 FDA reports)
BRONCHOPNEUMONIA ( 13 FDA reports)
CARDIAC TAMPONADE ( 13 FDA reports)
CAROTID BRUIT ( 13 FDA reports)
CHANGE OF BOWEL HABIT ( 13 FDA reports)
COLON ADENOMA ( 13 FDA reports)
CONCUSSION ( 13 FDA reports)
COORDINATION ABNORMAL ( 13 FDA reports)
DIFFICULTY IN WALKING ( 13 FDA reports)
DIVERTICULUM INTESTINAL ( 13 FDA reports)
DYSPLASTIC NAEVUS ( 13 FDA reports)
EAR DISCOMFORT ( 13 FDA reports)
EFFUSION ( 13 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 13 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 13 FDA reports)
ENDOCARDITIS ( 13 FDA reports)
EOSINOPHIL COUNT DECREASED ( 13 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 13 FDA reports)
GINGIVAL SWELLING ( 13 FDA reports)
GLOSSODYNIA ( 13 FDA reports)
HAND FRACTURE ( 13 FDA reports)
HEPATIC ENCEPHALOPATHY ( 13 FDA reports)
HEPATIC NEOPLASM ( 13 FDA reports)
HEPATOCELLULAR INJURY ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
IMPULSE-CONTROL DISORDER ( 13 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 13 FDA reports)
KELOID SCAR ( 13 FDA reports)
KERATOMILEUSIS ( 13 FDA reports)
LERICHE SYNDROME ( 13 FDA reports)
MIDDLE INSOMNIA ( 13 FDA reports)
NAIL OPERATION ( 13 FDA reports)
NEURITIS ( 13 FDA reports)
NODAL RHYTHM ( 13 FDA reports)
OCCULT BLOOD POSITIVE ( 13 FDA reports)
ORAL SURGERY ( 13 FDA reports)
ORGAN FAILURE ( 13 FDA reports)
PERICARDITIS ( 13 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 13 FDA reports)
PHOTOPHERESIS ( 13 FDA reports)
PHOTOPHOBIA ( 13 FDA reports)
PLATELET COUNT INCREASED ( 13 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 13 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 13 FDA reports)
PYELOCALIECTASIS ( 13 FDA reports)
PYLORIC STENOSIS ( 13 FDA reports)
RECTAL POLYP ( 13 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 13 FDA reports)
SARCOIDOSIS ( 13 FDA reports)
SINUS ARRHYTHMIA ( 13 FDA reports)
SKIN DISORDER ( 13 FDA reports)
SKIN HYPERTROPHY ( 13 FDA reports)
SPINAL DECOMPRESSION ( 13 FDA reports)
TIBIA FRACTURE ( 13 FDA reports)
ULCER ( 13 FDA reports)
URGE INCONTINENCE ( 13 FDA reports)
VAGINAL INFECTION ( 13 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 13 FDA reports)
VIITH NERVE PARALYSIS ( 13 FDA reports)
VITAMIN B12 DEFICIENCY ( 13 FDA reports)
VITAMIN D DEFICIENCY ( 13 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 13 FDA reports)
ABNORMAL FAECES ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 12 FDA reports)
ANXIETY DISORDER ( 12 FDA reports)
AORTIC CALCIFICATION ( 12 FDA reports)
APPENDIX DISORDER ( 12 FDA reports)
BILIARY TRACT DISORDER ( 12 FDA reports)
BIOPSY BONE MARROW ( 12 FDA reports)
BLADDER DYSFUNCTION ( 12 FDA reports)
BLADDER SPASM ( 12 FDA reports)
BLOOD MAGNESIUM DECREASED ( 12 FDA reports)
BONE NEOPLASM MALIGNANT ( 12 FDA reports)
BONE OPERATION ( 12 FDA reports)
BREAST LUMP REMOVAL ( 12 FDA reports)
BRONCHIOLITIS ( 12 FDA reports)
CARDIAC FAILURE ACUTE ( 12 FDA reports)
CERVICOBRACHIAL SYNDROME ( 12 FDA reports)
CHEST WALL OPERATION ( 12 FDA reports)
CONTRAST MEDIA REACTION ( 12 FDA reports)
DERMATITIS BULLOUS ( 12 FDA reports)
DYSPAREUNIA ( 12 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 12 FDA reports)
EXOPHTHALMOS ( 12 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 12 FDA reports)
FOOD ALLERGY ( 12 FDA reports)
FOOD INTOLERANCE ( 12 FDA reports)
GINGIVAL ATROPHY ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HEPATOSPLENOMEGALY ( 12 FDA reports)
HERNIA REPAIR ( 12 FDA reports)
HUNGER ( 12 FDA reports)
HYDROCEPHALUS ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 12 FDA reports)
HYSTERECTOMY ( 12 FDA reports)
ILIAC ARTERY THROMBOSIS ( 12 FDA reports)
IMPAIRED DRIVING ABILITY ( 12 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 12 FDA reports)
INGUINAL HERNIA ( 12 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 12 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 12 FDA reports)
JOINT ARTHROPLASTY ( 12 FDA reports)
KNEE ARTHROPLASTY ( 12 FDA reports)
LOSS OF LIBIDO ( 12 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 12 FDA reports)
LYMPHADENECTOMY ( 12 FDA reports)
MENISCUS REMOVAL ( 12 FDA reports)
METABOLIC DISORDER ( 12 FDA reports)
MONOCYTE COUNT DECREASED ( 12 FDA reports)
MYELOPATHY ( 12 FDA reports)
MYOCLONUS ( 12 FDA reports)
MYOPATHY ( 12 FDA reports)
NEOPLASM PROSTATE ( 12 FDA reports)
NEUTROPENIC SEPSIS ( 12 FDA reports)
NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
NON-CARDIAC CHEST PAIN ( 12 FDA reports)
OPTIC NEURITIS ( 12 FDA reports)
PANCREATITIS RELAPSING ( 12 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 12 FDA reports)
PLASTIC SURGERY ( 12 FDA reports)
PLEURAL CALCIFICATION ( 12 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 12 FDA reports)
POOR PERIPHERAL CIRCULATION ( 12 FDA reports)
POTENTIATING DRUG INTERACTION ( 12 FDA reports)
PROCEDURAL VOMITING ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
RIGHT ATRIAL DILATATION ( 12 FDA reports)
SALPINGITIS ( 12 FDA reports)
SCAB ( 12 FDA reports)
SEBACEOUS GLAND DISORDER ( 12 FDA reports)
SKULL MALFORMATION ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
SPINAL OPERATION ( 12 FDA reports)
SPINAL X-RAY ABNORMAL ( 12 FDA reports)
STEM CELL TRANSPLANT ( 12 FDA reports)
STOMACH DISCOMFORT ( 12 FDA reports)
TENDON DISORDER ( 12 FDA reports)
THINKING ABNORMAL ( 12 FDA reports)
VENOUS OCCLUSION ( 12 FDA reports)
VENTRICULAR DYSFUNCTION ( 12 FDA reports)
WOUND DRAINAGE ( 12 FDA reports)
ABDOMINAL ADHESIONS ( 11 FDA reports)
ABSCESS JAW ( 11 FDA reports)
ADNEXA UTERI MASS ( 11 FDA reports)
AFFECTIVE DISORDER ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
AORTIC DILATATION ( 11 FDA reports)
APPENDICITIS ( 11 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 11 FDA reports)
BREAST CANCER METASTATIC ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
CATARACT TRAUMATIC ( 11 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 11 FDA reports)
COSTOCHONDRITIS ( 11 FDA reports)
CRANIOSYNOSTOSIS ( 11 FDA reports)
CYSTITIS HAEMORRHAGIC ( 11 FDA reports)
DEAFNESS UNILATERAL ( 11 FDA reports)
DEFAECATION URGENCY ( 11 FDA reports)
DEVELOPMENTAL DELAY ( 11 FDA reports)
DIASTOLIC DYSFUNCTION ( 11 FDA reports)
DYSAESTHESIA ( 11 FDA reports)
ECZEMA INFECTED ( 11 FDA reports)
ELECTROLYTE IMBALANCE ( 11 FDA reports)
ENCEPHALITIS ( 11 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 11 FDA reports)
EPILEPSY ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
FEAR OF DEATH ( 11 FDA reports)
FEMORAL NECK FRACTURE ( 11 FDA reports)
GASTROINTESTINAL PERFORATION ( 11 FDA reports)
GLOBULINS INCREASED ( 11 FDA reports)
GYNAECOMASTIA ( 11 FDA reports)
HAIR GROWTH ABNORMAL ( 11 FDA reports)
HEPATIC CONGESTION ( 11 FDA reports)
HEPATIC ENZYME ABNORMAL ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
HEPATORENAL FAILURE ( 11 FDA reports)
HIV INFECTION ( 11 FDA reports)
HYPERAESTHESIA ( 11 FDA reports)
HYPOALBUMINAEMIA ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 11 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
LARYNGEAL OEDEMA ( 11 FDA reports)
LEFT VENTRICULAR FAILURE ( 11 FDA reports)
LEUKODYSTROPHY ( 11 FDA reports)
LHERMITTE'S SIGN ( 11 FDA reports)
LIP DRY ( 11 FDA reports)
LUNG INJURY ( 11 FDA reports)
LYME DISEASE ( 11 FDA reports)
LYMPH NODE PALPABLE ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
MECHANICAL VENTILATION ( 11 FDA reports)
MENTAL IMPAIRMENT ( 11 FDA reports)
MITRAL VALVE CALCIFICATION ( 11 FDA reports)
MUCOSAL HAEMORRHAGE ( 11 FDA reports)
MULTI-ORGAN DISORDER ( 11 FDA reports)
MYOCARDITIS ( 11 FDA reports)
OCULAR HYPERAEMIA ( 11 FDA reports)
OCULAR ICTERUS ( 11 FDA reports)
ONYCHALGIA ( 11 FDA reports)
ORAL MUCOSAL BLISTERING ( 11 FDA reports)
OTITIS MEDIA ACUTE ( 11 FDA reports)
OVARIAN MASS ( 11 FDA reports)
PANCREATIC CYST ( 11 FDA reports)
PARAPROTEINAEMIA ( 11 FDA reports)
PLEURAL FIBROSIS ( 11 FDA reports)
PSYCHIATRIC SYMPTOM ( 11 FDA reports)
RADICULITIS CERVICAL ( 11 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
RESPIRATORY ACIDOSIS ( 11 FDA reports)
RESPIRATORY TRACT CONGESTION ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SKIN OEDEMA ( 11 FDA reports)
SMALL INTESTINE OPERATION ( 11 FDA reports)
SOFT TISSUE DISORDER ( 11 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 11 FDA reports)
TONGUE DISCOLOURATION ( 11 FDA reports)
TONGUE DISORDER ( 11 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 11 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 11 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 11 FDA reports)
VASCULITIS ( 11 FDA reports)
VENTRICULAR DYSKINESIA ( 11 FDA reports)
VERTEBRAL COLUMN MASS ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
ABNORMAL SENSATION IN EYE ( 10 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 10 FDA reports)
AMYLOIDOSIS ( 10 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
ANAPHYLACTOID REACTION ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
APPETITE DISORDER ( 10 FDA reports)
ASPHYXIA ( 10 FDA reports)
ASPIRATION PLEURAL CAVITY ( 10 FDA reports)
ATRIAL TACHYCARDIA ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 10 FDA reports)
BENIGN BONE NEOPLASM ( 10 FDA reports)
BIFASCICULAR BLOCK ( 10 FDA reports)
BLADDER NEOPLASM ( 10 FDA reports)
BLOOD CHLORIDE INCREASED ( 10 FDA reports)
BLOOD IRON DECREASED ( 10 FDA reports)
BODY DYSMORPHIC DISORDER ( 10 FDA reports)
BONE FRAGMENTATION ( 10 FDA reports)
BRAIN HERNIATION ( 10 FDA reports)
CARBON DIOXIDE DECREASED ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 10 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 10 FDA reports)
CHOKING ( 10 FDA reports)
COLITIS ULCERATIVE ( 10 FDA reports)
CONDUCTION DISORDER ( 10 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 10 FDA reports)
CYSTIC FIBROSIS ( 10 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 10 FDA reports)
DENTURE WEARER ( 10 FDA reports)
DRUG DISPENSING ERROR ( 10 FDA reports)
DRY THROAT ( 10 FDA reports)
EAR DISORDER ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
EPICONDYLITIS ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
EXFOLIATIVE RASH ( 10 FDA reports)
EXTRASYSTOLES ( 10 FDA reports)
EYE PENETRATION ( 10 FDA reports)
FAILURE TO THRIVE ( 10 FDA reports)
FOOD POISONING ( 10 FDA reports)
GASTROINTESTINAL PAIN ( 10 FDA reports)
HEPATITIS CHOLESTATIC ( 10 FDA reports)
HODGKIN'S DISEASE ( 10 FDA reports)
IMMUNOGLOBULINS DECREASED ( 10 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
INTRA-UTERINE DEATH ( 10 FDA reports)
LARYNGITIS ( 10 FDA reports)
LIGAMENT INJURY ( 10 FDA reports)
LIP PAIN ( 10 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 10 FDA reports)
LUNG NEOPLASM MALIGNANT ( 10 FDA reports)
MANIA ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 10 FDA reports)
MUCOSAL ULCERATION ( 10 FDA reports)
MYDRIASIS ( 10 FDA reports)
NASAL SINUS CANCER ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NO ADVERSE EVENT ( 10 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 10 FDA reports)
PAPILLOMA VIRAL INFECTION ( 10 FDA reports)
PARALYTIC DISABILITY ( 10 FDA reports)
PHAEOCHROMOCYTOMA ( 10 FDA reports)
PRIMARY SEQUESTRUM ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 10 FDA reports)
SALIVARY GLAND ADENOMA ( 10 FDA reports)
SALPINGO-OOPHORECTOMY ( 10 FDA reports)
SEDATION ( 10 FDA reports)
SENSATION OF FOREIGN BODY ( 10 FDA reports)
SENSATION OF HEAVINESS ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
SKIN HYPERPIGMENTATION ( 10 FDA reports)
SOCIAL PROBLEM ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
TRISMUS ( 10 FDA reports)
TROPONIN INCREASED ( 10 FDA reports)
URETHRAL OBSTRUCTION ( 10 FDA reports)
URINARY HESITATION ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VASCULAR OPERATION ( 10 FDA reports)
VENOUS THROMBOSIS ( 10 FDA reports)
VERTIGO POSITIONAL ( 10 FDA reports)
WOUND INFECTION ( 10 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANAL PRURITUS ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
BACTERIAL DISEASE CARRIER ( 9 FDA reports)
BLEPHARITIS ( 9 FDA reports)
BLOOD BICARBONATE DECREASED ( 9 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 9 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 9 FDA reports)
BREAST PAIN ( 9 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
CATARACT NUCLEAR ( 9 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CHOREA ( 9 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 9 FDA reports)
CLAUSTROPHOBIA ( 9 FDA reports)
CLUMSINESS ( 9 FDA reports)
COLON OPERATION ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 9 FDA reports)
DEAFNESS BILATERAL ( 9 FDA reports)
DIABETIC KETOACIDOSIS ( 9 FDA reports)
DILATATION ATRIAL ( 9 FDA reports)
DROOLING ( 9 FDA reports)
DRUG LEVEL DECREASED ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 9 FDA reports)
EXCESSIVE EYE BLINKING ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
FISTULA REPAIR ( 9 FDA reports)
GANGRENE ( 9 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
GRANULOMA ( 9 FDA reports)
HAEMORRHAGIC ANAEMIA ( 9 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 9 FDA reports)
HELICOBACTER INFECTION ( 9 FDA reports)
HISTOPLASMOSIS ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPERNATRAEMIA ( 9 FDA reports)
HYPOPHOSPHATAEMIA ( 9 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
INCISIONAL HERNIA ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
JOINT LOCK ( 9 FDA reports)
JUGULAR VEIN DISTENSION ( 9 FDA reports)
JUGULAR VEIN THROMBOSIS ( 9 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 9 FDA reports)
LUNG TRANSPLANT REJECTION ( 9 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
NAIL DISCOLOURATION ( 9 FDA reports)
NAIL DYSTROPHY ( 9 FDA reports)
NAIL HYPERTROPHY ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
OPEN REDUCTION OF FRACTURE ( 9 FDA reports)
OROANTRAL FISTULA ( 9 FDA reports)
PANCREATITIS CHRONIC ( 9 FDA reports)
PARALYSIS ( 9 FDA reports)
PARAPARESIS ( 9 FDA reports)
PAROTITIS ( 9 FDA reports)
PERSONALITY CHANGE ( 9 FDA reports)
PNEUMONIA BACTERIAL ( 9 FDA reports)
PROTEIN URINE PRESENT ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
RADICAL MASTECTOMY ( 9 FDA reports)
RESIDUAL URINE ( 9 FDA reports)
RESUSCITATION ( 9 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 9 FDA reports)
SARCOMA ( 9 FDA reports)
SKIN FISSURES ( 9 FDA reports)
SMALL FOR DATES BABY ( 9 FDA reports)
STRIDOR ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
TENOSYNOVITIS STENOSANS ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
THROMBOSIS IN DEVICE ( 9 FDA reports)
TONSILLITIS ( 9 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 9 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 9 FDA reports)
URINARY TRACT OBSTRUCTION ( 9 FDA reports)
URTICARIA GENERALISED ( 9 FDA reports)
VASCULAR CALCIFICATION ( 9 FDA reports)
VISUAL DISTURBANCE ( 9 FDA reports)
ACARODERMATITIS ( 8 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 8 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ANAL HAEMORRHAGE ( 8 FDA reports)
ANOXIC ENCEPHALOPATHY ( 8 FDA reports)
APLASTIC ANAEMIA ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
ASTHMATIC CRISIS ( 8 FDA reports)
BABESIOSIS ( 8 FDA reports)
BACK INJURY ( 8 FDA reports)
BACTERIA STOOL IDENTIFIED ( 8 FDA reports)
BACTERIAL TEST ( 8 FDA reports)
BILIARY DILATATION ( 8 FDA reports)
BIOPSY LYMPH GLAND ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD BLISTER ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 8 FDA reports)
BRAIN DEATH ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CHOLECYSTITIS INFECTIVE ( 8 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 8 FDA reports)
CLEFT PALATE ( 8 FDA reports)
COLOSTOMY ( 8 FDA reports)
CORONARY ARTERY OCCLUSION ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DEVICE FAILURE ( 8 FDA reports)
DIABETES INSIPIDUS ( 8 FDA reports)
DIZZINESS POSTURAL ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
ECZEMA EYELIDS ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 8 FDA reports)
EXTREMITY CONTRACTURE ( 8 FDA reports)
FAMILY STRESS ( 8 FDA reports)
FAT NECROSIS ( 8 FDA reports)
FINGER DEFORMITY ( 8 FDA reports)
FLAT AFFECT ( 8 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HEPATIC TRAUMA ( 8 FDA reports)
HILAR LYMPHADENOPATHY ( 8 FDA reports)
HYPERALBUMINAEMIA ( 8 FDA reports)
HYPERLACTACIDAEMIA ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
INCISIONAL DRAINAGE ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
JAW DISORDER ( 8 FDA reports)
KAWASAKI'S DISEASE ( 8 FDA reports)
LACUNAR INFARCTION ( 8 FDA reports)
LIFE EXPECTANCY SHORTENED ( 8 FDA reports)
LOWER LIMB FRACTURE ( 8 FDA reports)
MASS EXCISION ( 8 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 8 FDA reports)
MAXILLOFACIAL OPERATION ( 8 FDA reports)
MEDICAL DEVICE REMOVAL ( 8 FDA reports)
MENORRHAGIA ( 8 FDA reports)
MICROCYTIC ANAEMIA ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MUSCLE RIGIDITY ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
NEPHROPATHY ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 8 FDA reports)
ONYCHOMADESIS ( 8 FDA reports)
PERICARDIAL HAEMORRHAGE ( 8 FDA reports)
PIERRE ROBIN SYNDROME ( 8 FDA reports)
PNEUMONIA FUNGAL ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
POOR PERSONAL HYGIENE ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
PORTAL HYPERTENSION ( 8 FDA reports)
POSTNASAL DRIP ( 8 FDA reports)
PROCEDURAL NAUSEA ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 8 FDA reports)
PULMONARY TUBERCULOSIS ( 8 FDA reports)
PYURIA ( 8 FDA reports)
RED BLOOD CELL ABNORMALITY ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 8 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 8 FDA reports)
RENAL TUBULAR DISORDER ( 8 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
RIGHT VENTRICULAR FAILURE ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
SCLERAL HAEMORRHAGE ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SPINAL CORD DISORDER ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
SUTURE RUPTURE ( 8 FDA reports)
SYNOVITIS ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
TEARFULNESS ( 8 FDA reports)
THROMBOCYTOSIS ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TOOTH DEPOSIT ( 8 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 8 FDA reports)
VANISHING BILE DUCT SYNDROME ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
VENA CAVA FILTER INSERTION ( 8 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 8 FDA reports)
VERTEBROPLASTY ( 8 FDA reports)
VIRAL LABYRINTHITIS ( 8 FDA reports)
VIRAL PHARYNGITIS ( 8 FDA reports)
VITAMIN B12 DECREASED ( 8 FDA reports)
VITREOUS DETACHMENT ( 8 FDA reports)
ACINETOBACTER INFECTION ( 7 FDA reports)
ACUTE CHEST SYNDROME ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
ADVERSE REACTION ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
ALVEOLITIS ALLERGIC ( 7 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 7 FDA reports)
AORTIC VALVE SCLEROSIS ( 7 FDA reports)
APICECTOMY ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
APPLICATION SITE BURN ( 7 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BONE MARROW TRANSPLANT ( 7 FDA reports)
BONE METABOLISM DISORDER ( 7 FDA reports)
BRAIN INJURY ( 7 FDA reports)
BREAST CANCER RECURRENT ( 7 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CALCULUS URETERIC ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CAROTID ARTERY DISEASE ( 7 FDA reports)
CATHETER RELATED INFECTION ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 7 FDA reports)
CHONDROCALCINOSIS ( 7 FDA reports)
CLUSTER HEADACHE ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
CONJUNCTIVITIS VIRAL ( 7 FDA reports)
CORYNEBACTERIUM INFECTION ( 7 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
DENTAL FISTULA ( 7 FDA reports)
DENTAL PLAQUE ( 7 FDA reports)
DIAPHRAGMATIC INJURY ( 7 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
EPIDURAL LIPOMATOSIS ( 7 FDA reports)
ESCHAR ( 7 FDA reports)
EYE DISCHARGE ( 7 FDA reports)
FACET JOINT BLOCK ( 7 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 7 FDA reports)
FOLATE DEFICIENCY ( 7 FDA reports)
GASTROINTESTINAL INJURY ( 7 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 7 FDA reports)
GINGIVAL ABSCESS ( 7 FDA reports)
GINGIVAL EROSION ( 7 FDA reports)
GINGIVAL OEDEMA ( 7 FDA reports)
GLOSSITIS ( 7 FDA reports)
GRAFT INFECTION ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HAND DEFORMITY ( 7 FDA reports)
HEPATIC INFECTION FUNGAL ( 7 FDA reports)
HOSPICE CARE ( 7 FDA reports)
HYPERACUSIS ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
HYPOGEUSIA ( 7 FDA reports)
INCISION SITE PAIN ( 7 FDA reports)
INTESTINAL POLYP ( 7 FDA reports)
ISCHAEMIC HEPATITIS ( 7 FDA reports)
LOCALISED INFECTION ( 7 FDA reports)
LUNG OPERATION ( 7 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
MENINGIOMA ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
METAPLASIA ( 7 FDA reports)
METASTASES TO PANCREAS ( 7 FDA reports)
METASTASES TO SPLEEN ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MOUTH INJURY ( 7 FDA reports)
MYCOPLASMA INFECTION ( 7 FDA reports)
NASAL DISORDER ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEPHRITIS ( 7 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 7 FDA reports)
NEUROPATHY ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OTITIS MEDIA CHRONIC ( 7 FDA reports)
OTOTOXICITY ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PANIC DISORDER ( 7 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 7 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 7 FDA reports)
PERIARTHRITIS ( 7 FDA reports)
PERIODONTAL OPERATION ( 7 FDA reports)
PERIRECTAL ABSCESS ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PLEURAL ADHESION ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
PROSTATISM ( 7 FDA reports)
PSYCHOLOGICAL TRAUMA ( 7 FDA reports)
SENSORY LOSS ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SKIN PLAQUE ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 7 FDA reports)
SUICIDAL BEHAVIOUR ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 7 FDA reports)
VAGINITIS BACTERIAL ( 7 FDA reports)
VASCULAR DEMENTIA ( 7 FDA reports)
XEROSIS ( 7 FDA reports)
ABORTION MISSED ( 6 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
ALCOHOL ABUSE ( 6 FDA reports)
ALCOHOL USE ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
AMINO ACID LEVEL INCREASED ( 6 FDA reports)
AORTIC DISORDER ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
APHONIA ( 6 FDA reports)
ARTERIAL BYPASS OPERATION ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 6 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 6 FDA reports)
BLOOD PRESSURE ABNORMAL ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BONE MARROW DISORDER ( 6 FDA reports)
BURNING MOUTH SYNDROME ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
CARDIAC FLUTTER ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CATHETER RELATED COMPLICATION ( 6 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CORONARY ARTERY THROMBOSIS ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
CUTANEOUS SARCOIDOSIS ( 6 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 6 FDA reports)
DEPENDENCE ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 6 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
ENTHESOPATHY ( 6 FDA reports)
EROSIVE OESOPHAGITIS ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
GUN SHOT WOUND ( 6 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HEART RATE ABNORMAL ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HYPERAMYLASAEMIA ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
HYPOPNOEA ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
INFECTED DERMAL CYST ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
INITIAL INSOMNIA ( 6 FDA reports)
KLEBSIELLA INFECTION ( 6 FDA reports)
LARGE INTESTINAL ULCER ( 6 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
LORDOSIS ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MASTOIDITIS ( 6 FDA reports)
MEDIASTINAL MASS ( 6 FDA reports)
MEGACOLON ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
NASAL OBSTRUCTION ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 6 FDA reports)
OBSTRUCTION GASTRIC ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OESOPHAGEAL DISORDER ( 6 FDA reports)
OPPORTUNISTIC INFECTION ( 6 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 6 FDA reports)
OVARIAN ENLARGEMENT ( 6 FDA reports)
PALATAL DISORDER ( 6 FDA reports)
PANCREATIC ENZYMES INCREASED ( 6 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PENILE HAEMORRHAGE ( 6 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 6 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 6 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 6 FDA reports)
PREMATURE LABOUR ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PRODUCT TASTE ABNORMAL ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
PSEUDOMONAL SEPSIS ( 6 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 6 FDA reports)
PULMONARY CAVITATION ( 6 FDA reports)
RADIUS FRACTURE ( 6 FDA reports)
RECTAL PROLAPSE ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 6 FDA reports)
RETINAL TEAR ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SKELETAL INJURY ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN SWELLING ( 6 FDA reports)
SLEEP TALKING ( 6 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STATUS ASTHMATICUS ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
TONGUE PARALYSIS ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TOXOPLASMOSIS ( 6 FDA reports)
TRACHEOBRONCHITIS ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 6 FDA reports)
WEIGHT BEARING DIFFICULTY ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
WOUND HAEMORRHAGE ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ACUTE PSYCHOSIS ( 5 FDA reports)
ACUTE TONSILLITIS ( 5 FDA reports)
ADRENAL SUPPRESSION ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 5 FDA reports)
ANAL INFLAMMATION ( 5 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
AXILLARY MASS ( 5 FDA reports)
BACTERIURIA ( 5 FDA reports)
BLADDER PROLAPSE ( 5 FDA reports)
BLEPHAROSPASM ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD PH INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BREAST MASS ( 5 FDA reports)
BRONCHIAL SECRETION RETENTION ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
BRONCHITIS CHRONIC ( 5 FDA reports)
BRONCHOMALACIA ( 5 FDA reports)
BUNION ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CATHETERISATION VENOUS ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 5 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 5 FDA reports)
CLONIC CONVULSION ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
CULTURE POSITIVE ( 5 FDA reports)
CYTOKINE RELEASE SYNDROME ( 5 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 5 FDA reports)
DIABETIC COMA ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSPHEMIA ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
EMBOLISM VENOUS ( 5 FDA reports)
EMPYEMA ( 5 FDA reports)
ENDOCRINE DISORDER ( 5 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 5 FDA reports)
ETHMOID SINUS SURGERY ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
EYES SUNKEN ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FAT INTOLERANCE ( 5 FDA reports)
FEEDING DISORDER NEONATAL ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
FULL BLOOD COUNT DECREASED ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTRODUODENITIS ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 5 FDA reports)
HAEMOBILIA ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INGUINAL MASS ( 5 FDA reports)
INTERCOSTAL NEURALGIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
LARYNGOCELE ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LIMB DEFORMITY ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MENINGISM ( 5 FDA reports)
MENINGOMYELOCELE ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METASTATIC GASTRIC CANCER ( 5 FDA reports)
MUCOSAL DRYNESS ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
MYOPIA ( 5 FDA reports)
NARCOLEPSY ( 5 FDA reports)
NECK INJURY ( 5 FDA reports)
NEOPLASM ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 5 FDA reports)
PCO2 DECREASED ( 5 FDA reports)
PELVIC ABSCESS ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 5 FDA reports)
PERITONSILLAR ABSCESS ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
POLYCYTHAEMIA ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 5 FDA reports)
PROSTATOMEGALY ( 5 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 5 FDA reports)
RENAL HYPERTROPHY ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RENAL TUBULAR ACIDOSIS ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RHINITIS SEASONAL ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SICCA SYNDROME ( 5 FDA reports)
SINUS ANTROSTOMY ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
SPINA BIFIDA ( 5 FDA reports)
STRESS INCONTINENCE ( 5 FDA reports)
STRESS ULCER ( 5 FDA reports)
STRESS URINARY INCONTINENCE ( 5 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 5 FDA reports)
TENDON INJURY ( 5 FDA reports)
TINEA CRURIS ( 5 FDA reports)
TRAUMATIC SHOCK ( 5 FDA reports)
TRICUSPID VALVE DISEASE ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
TUBERCULOUS PLEURISY ( 5 FDA reports)
TUMOUR FLARE ( 5 FDA reports)
TURNER'S SYNDROME ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
URTICARIA PAPULAR ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENOUS STENOSIS ( 5 FDA reports)
VERTEBRAL WEDGING ( 5 FDA reports)
VIRAL RASH ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
ABDOMINAL INJURY ( 4 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AIDS ENCEPHALOPATHY ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALLERGY TEST POSITIVE ( 4 FDA reports)
ALLERGY TO ANIMAL ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
APPLICATION SITE PRURITUS ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
APTYALISM ( 4 FDA reports)
ASPERGILLOMA ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BK VIRUS INFECTION ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
BREAST CALCIFICATIONS ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
CAECITIS ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CARCINOID SYNDROME ( 4 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CATAPLEXY ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHONDROMALACIA ( 4 FDA reports)
CHOREOATHETOSIS ( 4 FDA reports)
CHORIOAMNIONITIS ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CHRONIC TONSILLITIS ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYSTIC FIBROSIS RELATED DIABETES ( 4 FDA reports)
CYTOGENETIC ABNORMALITY ( 4 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
DARK CIRCLES UNDER EYES ( 4 FDA reports)
DAYDREAMING ( 4 FDA reports)
DELAYED SLEEP PHASE ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIABETIC NEPHROPATHY ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DUODENAL STENOSIS ( 4 FDA reports)
EARLY SATIETY ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EXOMPHALOS ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FACIAL WASTING ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEEDING PROBLEM IN CHILD ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
FRACTURE NONUNION ( 4 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GENE MUTATION ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
GRIP STRENGTH DECREASED ( 4 FDA reports)
GROWTH RETARDATION ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPATIC VEIN THROMBOSIS ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
ILIAC ARTERY STENOSIS ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFERIOR VENA CAVA DILATATION ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
ISOSPORIASIS ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
LAZINESS ( 4 FDA reports)
LEARNING DISABILITY ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MEDIASTINAL BIOPSY ( 4 FDA reports)
MEDIASTINAL CYST ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 4 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
NEUROENDOCRINE TUMOUR ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PENICILLIOSIS ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PHYSIOTHERAPY ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PINGUECULA ( 4 FDA reports)
PLASMACYTOSIS ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
PREGNANCY TEST POSITIVE ( 4 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 4 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 4 FDA reports)
REFLUX LARYNGITIS ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RENAL TRANSPLANT ( 4 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 4 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
ROTAVIRUS INFECTION ( 4 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 4 FDA reports)
SCAN BONE MARROW ABNORMAL ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SOFT TISSUE MASS ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL CORD INJURY CERVICAL ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STOMACH MASS ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRONGYLOIDIASIS ( 4 FDA reports)
SUBCUTANEOUS NODULE ( 4 FDA reports)
SYPHILIS ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
TENSION ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THYMOMA ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VENOUS INJURY ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VIRAEMIA ( 4 FDA reports)
VISCERAL LEISHMANIASIS ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADRENALITIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALLERGIC PHARYNGITIS ( 3 FDA reports)
ALLERGY TEST ( 3 FDA reports)
ANAEMIA POSTOPERATIVE ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
APATHY ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BEREAVEMENT REACTION ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLADDER DILATATION ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLAST CELL COUNT DECREASED ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST HAEMATOMA ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
CALCIPHYLAXIS ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CARBON DIOXIDE ABNORMAL ( 3 FDA reports)
CARDIAC AMYLOIDOSIS ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHILD NEGLECT ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
CONJUNCTIVAL DISORDER ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CRANIOCEREBRAL INJURY ( 3 FDA reports)
CYSTIC FIBROSIS LUNG ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIAPHRAGMATIC HERNIA ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DUCTUS ARTERIOSUS STENOSIS FOETAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
END STAGE AIDS ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FRACTURE DISPLACEMENT ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
FUNISITIS ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROSCHISIS ( 3 FDA reports)
GENERAL SYMPTOM ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GIARDIASIS ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HEPATIC ATROPHY ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERNIA CONGENITAL ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
HYPOSPADIAS ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON METABOLISM DISORDER ( 3 FDA reports)
IRREGULAR SLEEP PHASE ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LARYNGOMALACIA ( 3 FDA reports)
LARYNGOTRACHEITIS ( 3 FDA reports)
LDL/HDL RATIO DECREASED ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIMB REDUCTION DEFECT ( 3 FDA reports)
LINEAR IGA DISEASE ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
LYMPH NODE ABSCESS ( 3 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MACULAR FIBROSIS ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOANING ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYELOMA RECURRENCE ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NASAL SEPTUM PERFORATION ( 3 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 3 FDA reports)
NEONATAL ASPIRATION ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OESOPHAGEAL RUPTURE ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OVARIAN CYST RUPTURED ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 3 FDA reports)
PINEAL GLAND CYST ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PLEURAL HAEMORRHAGE ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POSITIONAL PLAGIOCEPHALY ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTOPERATIVE FEVER ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 3 FDA reports)
PRODUCT LABEL ISSUE ( 3 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 3 FDA reports)
PROLONGED EXPIRATION ( 3 FDA reports)
PROSTATIC CALCIFICATION ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SKIN LESION EXCISION ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPINE MALFORMATION ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
SWEAT DISCOLOURATION ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
THALASSAEMIA ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
TWIN PREGNANCY ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URETHRAL DISCHARGE ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
VAGINITIS ATROPHIC ( 3 FDA reports)
VASCULITIC RASH ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VOMITING IN PREGNANCY ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
VULVITIS ( 3 FDA reports)
WEIGHT GAIN POOR ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
17-HYDROXYPROGESTERONE INCREASED ( 2 FDA reports)
ABORTION INCOMPLETE ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALCOHOLIC PSYCHOSIS ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL FISTULA INFECTION ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BILE OUTPUT ABNORMAL ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD HIV RNA INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURKHOLDERIA TEST POSITIVE ( 2 FDA reports)
CARCINOMA IN SITU OF SKIN ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CONGENITAL MEGACOLON ( 2 FDA reports)
CONGENITAL NOSE MALFORMATION ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CRANIAL SUTURES WIDENING ( 2 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL NECROSIS ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSTROPHIA MYOTONICA ( 2 FDA reports)
ECHOVIRUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENTEROCELE ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EVANS SYNDROME ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FISSURE OF TONGUE, CONGENITAL ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUOROSIS ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL CANDIDIASIS ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GONORRHOEA ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPLANT SITE ERYTHEMA ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTION REACTIVATION ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRAUTERINE INFECTION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KLEPTOMANIA ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEMIERRE SYNDROME ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOGRANULOMA ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MECONIUM ABNORMAL ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MICROGNATHIA ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MITRAL VALVE ATRESIA ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PATHOLOGICAL GAMBLING ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POPLITEAL PULSE DECREASED ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PRECOCIOUS PUBERTY ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 2 FDA reports)
PROCTITIS HERPES ( 2 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRODUCT PACKAGING ISSUE ( 2 FDA reports)
PROMOTION OF WOUND HEALING ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RASH FOLLICULAR ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SPLEEN PALPABLE ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUDDEN VISUAL LOSS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
UREAPLASMA INFECTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
VENTRICULAR HYPOPLASIA ( 2 FDA reports)
VESSEL PUNCTURE SITE SWELLING ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVAL ERYTHEMA ( 2 FDA reports)
VULVOVAGINITIS ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
XANTHELASMA ( 2 FDA reports)
XYY SYNDROME ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENOGENITAL SYNDROME ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AIDS CHOLANGIOPATHY ( 1 FDA reports)
AIDS RELATED COMPLEX ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTHENOSPERMIA ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE DEFICIENCY SYNDROME ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BORDERLINE LEPROSY ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHITIS CHEMICAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CANDIDA NAPPY RASH ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHLAMYDIA IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL STAINING ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COXSACKIE MYOCARDITIS ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS MYELOMENINGORADICULITIS ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DEVICE SIGNAL DETECTION ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DIFFUSE VASCULITIS ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG CLEARANCE INCREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EUSTACHIAN TUBE STENOSIS ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FITZ-HUGH-CURTIS SYNDROME ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLAVIVIRUS TEST POSITIVE ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRADENIGO'S SYNDROME ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROUP B STREPTOCOCCUS NEONATAL SEPSIS ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCHROMASIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPERVITAMINOSIS D ( 1 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNE AGGLUTININS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSTILLATION SITE REACTION ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
ISOLATED ADRENOCORTICOTROPIC HORMONE DEFICIENCY ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LABYRINTHINE FISTULA ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEISHMANIASIS ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER FUNCTION TEST NORMAL ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS HERPES ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUMPS ANTIBODY TEST POSITIVE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDITIS BACTERIAL ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEONATAL RESPIRATORY ARREST ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURILEMMOMA MALIGNANT ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
OBSTRUCTED LABOUR ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULOFACIAL PARALYSIS ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OFFICE VISIT ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSMOLAR GAP ABNORMAL ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOLOGY TEST ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL NECROSIS ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLATELET FACTOR 4 ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POROKERATOSIS ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POST-TUSSIVE VOMITING ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIMARY HYPOTHYROIDISM ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYLOROMYOTOMY ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SALIVA ALCOHOL TEST POSITIVE ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAPHOCEPHALY ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLE ARTHRITIS ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBACUTE HEPATIC FAILURE ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TERATOSPERMIA ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THERMOANAESTHESIA ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYMOMA MALIGNANT ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE PRURITUS ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TUBERCULOID LEPROSY ( 1 FDA reports)
TUBERCULOSIS OF INTRATHORACIC LYMPH NODES ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINITIS CHLAMYDIAL ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR PRE-EXCITATION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRUS BODY FLUID IDENTIFIED ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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