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

PYREXIA ( 1051 FDA reports)
PAIN ( 906 FDA reports)
DIARRHOEA ( 883 FDA reports)
DYSPNOEA ( 846 FDA reports)
NAUSEA ( 785 FDA reports)
VOMITING ( 761 FDA reports)
ANAEMIA ( 730 FDA reports)
ANXIETY ( 721 FDA reports)
OSTEONECROSIS OF JAW ( 630 FDA reports)
PRURITUS ( 609 FDA reports)
FATIGUE ( 579 FDA reports)
PNEUMONIA ( 573 FDA reports)
RASH ( 563 FDA reports)
ASTHENIA ( 560 FDA reports)
ABDOMINAL PAIN ( 537 FDA reports)
RENAL FAILURE ACUTE ( 515 FDA reports)
BACK PAIN ( 479 FDA reports)
INJURY ( 476 FDA reports)
WEIGHT DECREASED ( 476 FDA reports)
HYPOTENSION ( 454 FDA reports)
OEDEMA PERIPHERAL ( 453 FDA reports)
THROMBOCYTOPENIA ( 448 FDA reports)
ERYTHEMA ( 431 FDA reports)
BONE DISORDER ( 423 FDA reports)
ARTHRALGIA ( 422 FDA reports)
CHEST PAIN ( 421 FDA reports)
DEPRESSION ( 410 FDA reports)
HEADACHE ( 401 FDA reports)
FALL ( 390 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 382 FDA reports)
OSTEOMYELITIS ( 380 FDA reports)
JAUNDICE ( 379 FDA reports)
SINUSITIS ( 376 FDA reports)
DIZZINESS ( 370 FDA reports)
MALAISE ( 357 FDA reports)
OSTEOARTHRITIS ( 357 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 354 FDA reports)
PLEURAL EFFUSION ( 342 FDA reports)
CELLULITIS ( 338 FDA reports)
PAIN IN JAW ( 337 FDA reports)
COUGH ( 336 FDA reports)
URINARY TRACT INFECTION ( 333 FDA reports)
PAIN IN EXTREMITY ( 332 FDA reports)
HYPERTENSION ( 328 FDA reports)
HYPOAESTHESIA ( 328 FDA reports)
DEHYDRATION ( 327 FDA reports)
DYSPHAGIA ( 327 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 321 FDA reports)
NEUROPATHY PERIPHERAL ( 321 FDA reports)
RENAL FAILURE ( 317 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 316 FDA reports)
CONFUSIONAL STATE ( 309 FDA reports)
URTICARIA ( 309 FDA reports)
EMOTIONAL DISTRESS ( 300 FDA reports)
PANCYTOPENIA ( 293 FDA reports)
CONSTIPATION ( 288 FDA reports)
NEUTROPENIA ( 288 FDA reports)
ATELECTASIS ( 287 FDA reports)
INFECTION ( 281 FDA reports)
SPINAL OSTEOARTHRITIS ( 279 FDA reports)
SEPSIS ( 274 FDA reports)
TOOTH EXTRACTION ( 272 FDA reports)
BRONCHITIS ( 265 FDA reports)
DRUG INTERACTION ( 263 FDA reports)
ANAPHYLACTIC SHOCK ( 260 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 257 FDA reports)
PARAESTHESIA ( 256 FDA reports)
DEEP VEIN THROMBOSIS ( 249 FDA reports)
TOXIC SKIN ERUPTION ( 248 FDA reports)
CHILLS ( 246 FDA reports)
TACHYCARDIA ( 243 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 242 FDA reports)
PULMONARY EMBOLISM ( 241 FDA reports)
VISION BLURRED ( 236 FDA reports)
DECREASED APPETITE ( 235 FDA reports)
DEATH ( 234 FDA reports)
LYMPHADENOPATHY ( 233 FDA reports)
ABDOMINAL PAIN UPPER ( 232 FDA reports)
HAEMATURIA ( 232 FDA reports)
MYOCARDIAL INFARCTION ( 231 FDA reports)
RASH MACULO-PAPULAR ( 228 FDA reports)
INSOMNIA ( 227 FDA reports)
HEPATITIS ( 223 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 223 FDA reports)
OSTEOPENIA ( 223 FDA reports)
ATRIAL FIBRILLATION ( 221 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 221 FDA reports)
SWELLING ( 215 FDA reports)
ANHEDONIA ( 212 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 211 FDA reports)
HYPERHIDROSIS ( 206 FDA reports)
CARDIOMEGALY ( 205 FDA reports)
NECK PAIN ( 203 FDA reports)
BLOOD BILIRUBIN INCREASED ( 201 FDA reports)
OSTEOPOROSIS ( 201 FDA reports)
HEPATITIS CHOLESTATIC ( 199 FDA reports)
CORONARY ARTERY DISEASE ( 197 FDA reports)
CHOLESTASIS ( 195 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 195 FDA reports)
HYPERSENSITIVITY ( 195 FDA reports)
RESPIRATORY FAILURE ( 195 FDA reports)
CHOLELITHIASIS ( 193 FDA reports)
SYNCOPE ( 193 FDA reports)
DRUG INEFFECTIVE ( 191 FDA reports)
IMPAIRED HEALING ( 188 FDA reports)
INFLAMMATION ( 180 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 180 FDA reports)
FACE OEDEMA ( 179 FDA reports)
HAEMOGLOBIN DECREASED ( 179 FDA reports)
BONE PAIN ( 178 FDA reports)
BLOOD CREATININE INCREASED ( 175 FDA reports)
DEFORMITY ( 175 FDA reports)
GAIT DISTURBANCE ( 175 FDA reports)
LEUKOPENIA ( 175 FDA reports)
DENTAL CARIES ( 174 FDA reports)
MUSCLE SPASMS ( 174 FDA reports)
OEDEMA ( 174 FDA reports)
SKIN LESION ( 174 FDA reports)
GASTRITIS ( 173 FDA reports)
LOSS OF CONSCIOUSNESS ( 172 FDA reports)
CONDITION AGGRAVATED ( 171 FDA reports)
MULTIPLE MYELOMA ( 170 FDA reports)
HYPOKALAEMIA ( 169 FDA reports)
MUSCULAR WEAKNESS ( 169 FDA reports)
DECREASED INTEREST ( 168 FDA reports)
MYALGIA ( 164 FDA reports)
HAEMORRHOIDS ( 162 FDA reports)
BONE LESION ( 161 FDA reports)
EOSINOPHILIA ( 161 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 161 FDA reports)
RECTAL HAEMORRHAGE ( 160 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 160 FDA reports)
TOOTH ABSCESS ( 158 FDA reports)
DIVERTICULUM ( 157 FDA reports)
CARDIAC ARREST ( 156 FDA reports)
CEREBROVASCULAR ACCIDENT ( 156 FDA reports)
CONVULSION ( 156 FDA reports)
EXOSTOSIS ( 156 FDA reports)
LUNG DISORDER ( 156 FDA reports)
LEUKOCYTOSIS ( 155 FDA reports)
MOUTH ULCERATION ( 155 FDA reports)
SKIN EXFOLIATION ( 154 FDA reports)
SWELLING FACE ( 154 FDA reports)
HIATUS HERNIA ( 153 FDA reports)
HYPERLIPIDAEMIA ( 153 FDA reports)
BLOOD GLUCOSE INCREASED ( 151 FDA reports)
HYPONATRAEMIA ( 151 FDA reports)
HEPATIC ENZYME INCREASED ( 149 FDA reports)
RASH ERYTHEMATOUS ( 149 FDA reports)
SEPTIC SHOCK ( 148 FDA reports)
DYSPEPSIA ( 147 FDA reports)
NEOPLASM MALIGNANT ( 147 FDA reports)
DISABILITY ( 145 FDA reports)
MUSCULOSKELETAL PAIN ( 144 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 143 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 143 FDA reports)
SOMNOLENCE ( 143 FDA reports)
AGRANULOCYTOSIS ( 142 FDA reports)
RASH GENERALISED ( 142 FDA reports)
STOMATITIS ( 142 FDA reports)
BRONCHOSPASM ( 141 FDA reports)
PURPURA ( 140 FDA reports)
STEVENS-JOHNSON SYNDROME ( 140 FDA reports)
ASTHMA ( 138 FDA reports)
DRUG HYPERSENSITIVITY ( 138 FDA reports)
OSTEITIS ( 138 FDA reports)
HYPOXIA ( 137 FDA reports)
PULMONARY OEDEMA ( 137 FDA reports)
HERPES ZOSTER ( 136 FDA reports)
SPINAL COMPRESSION FRACTURE ( 136 FDA reports)
ANAPHYLACTIC REACTION ( 134 FDA reports)
CYTOLYTIC HEPATITIS ( 134 FDA reports)
CHEST DISCOMFORT ( 131 FDA reports)
DISORIENTATION ( 130 FDA reports)
RENAL FAILURE CHRONIC ( 130 FDA reports)
GINGIVITIS ( 129 FDA reports)
CATARACT ( 127 FDA reports)
DIABETES MELLITUS ( 127 FDA reports)
OVERDOSE ( 127 FDA reports)
ARTERIOSCLEROSIS ( 125 FDA reports)
TREMOR ( 125 FDA reports)
MITRAL VALVE INCOMPETENCE ( 124 FDA reports)
NEPHROLITHIASIS ( 124 FDA reports)
VERTIGO ( 123 FDA reports)
ABDOMINAL DISTENSION ( 122 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 122 FDA reports)
SINUS DISORDER ( 122 FDA reports)
CANDIDIASIS ( 121 FDA reports)
MUCOSAL INFLAMMATION ( 119 FDA reports)
HEPATIC FAILURE ( 118 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 117 FDA reports)
LUNG NEOPLASM ( 117 FDA reports)
PALPITATIONS ( 117 FDA reports)
RESPIRATORY DISTRESS ( 117 FDA reports)
MULTI-ORGAN FAILURE ( 115 FDA reports)
ARTHROPATHY ( 114 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 113 FDA reports)
HAEMATOCHEZIA ( 113 FDA reports)
MASTICATION DISORDER ( 112 FDA reports)
OSTEONECROSIS ( 112 FDA reports)
WEIGHT INCREASED ( 112 FDA reports)
TOOTHACHE ( 111 FDA reports)
GENERALISED ERYTHEMA ( 110 FDA reports)
METASTASES TO BONE ( 110 FDA reports)
CHROMATURIA ( 109 FDA reports)
ARTHRITIS ( 108 FDA reports)
FEBRILE NEUTROPENIA ( 108 FDA reports)
STAPHYLOCOCCAL INFECTION ( 107 FDA reports)
DEBRIDEMENT ( 106 FDA reports)
DERMATITIS EXFOLIATIVE ( 105 FDA reports)
CARDIAC DISORDER ( 104 FDA reports)
HYPERGLYCAEMIA ( 104 FDA reports)
ANGIOEDEMA ( 103 FDA reports)
BLISTER ( 103 FDA reports)
SINUS TACHYCARDIA ( 103 FDA reports)
SKIN DISORDER ( 102 FDA reports)
NASAL CONGESTION ( 101 FDA reports)
COMPRESSION FRACTURE ( 100 FDA reports)
LIVER DISORDER ( 100 FDA reports)
EPISTAXIS ( 99 FDA reports)
HEPATIC STEATOSIS ( 99 FDA reports)
OSTEOLYSIS ( 99 FDA reports)
ANOREXIA ( 98 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 98 FDA reports)
EAR PAIN ( 98 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 98 FDA reports)
COLITIS ( 97 FDA reports)
HYPOPHAGIA ( 97 FDA reports)
ROTATOR CUFF SYNDROME ( 97 FDA reports)
SCOLIOSIS ( 97 FDA reports)
TOOTH DISORDER ( 97 FDA reports)
CARDIAC FAILURE ( 95 FDA reports)
FISTULA ( 95 FDA reports)
RENAL CYST ( 95 FDA reports)
SLEEP APNOEA SYNDROME ( 95 FDA reports)
AGITATION ( 94 FDA reports)
ASCITES ( 94 FDA reports)
HYPERKALAEMIA ( 94 FDA reports)
JAW FRACTURE ( 94 FDA reports)
ORAL DISORDER ( 94 FDA reports)
PRIMARY SEQUESTRUM ( 94 FDA reports)
TRANSAMINASES INCREASED ( 94 FDA reports)
OLIGURIA ( 93 FDA reports)
CONTUSION ( 92 FDA reports)
MENTAL STATUS CHANGES ( 92 FDA reports)
ORAL CANDIDIASIS ( 92 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 92 FDA reports)
DYSURIA ( 91 FDA reports)
PRODUCT QUALITY ISSUE ( 91 FDA reports)
CARPAL TUNNEL SYNDROME ( 90 FDA reports)
DYSPNOEA EXERTIONAL ( 89 FDA reports)
PLATELET COUNT DECREASED ( 89 FDA reports)
RASH PUSTULAR ( 89 FDA reports)
BALANCE DISORDER ( 88 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 88 FDA reports)
GINGIVAL SWELLING ( 88 FDA reports)
ENDODONTIC PROCEDURE ( 87 FDA reports)
DISCOMFORT ( 86 FDA reports)
NEURALGIA ( 86 FDA reports)
TOOTH LOSS ( 86 FDA reports)
WHEEZING ( 86 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 85 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 84 FDA reports)
ANGINA PECTORIS ( 84 FDA reports)
BONE MARROW FAILURE ( 84 FDA reports)
HEPATOMEGALY ( 84 FDA reports)
HOT FLUSH ( 84 FDA reports)
MIGRAINE ( 84 FDA reports)
PERIODONTAL DISEASE ( 84 FDA reports)
PULMONARY HYPERTENSION ( 84 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 83 FDA reports)
BLOOD PRESSURE DECREASED ( 83 FDA reports)
MELAENA ( 83 FDA reports)
HEART RATE INCREASED ( 82 FDA reports)
HYPOGLYCAEMIA ( 82 FDA reports)
LUMBAR SPINAL STENOSIS ( 82 FDA reports)
OXYGEN SATURATION DECREASED ( 82 FDA reports)
RIB FRACTURE ( 82 FDA reports)
SKIN ULCER ( 82 FDA reports)
URINARY INCONTINENCE ( 82 FDA reports)
EMPHYSEMA ( 81 FDA reports)
OESOPHAGITIS ( 81 FDA reports)
HAEMATOMA ( 80 FDA reports)
ORAL PAIN ( 80 FDA reports)
ALOPECIA ( 79 FDA reports)
ECZEMA ( 79 FDA reports)
ERECTILE DYSFUNCTION ( 79 FDA reports)
INTERSTITIAL LUNG DISEASE ( 79 FDA reports)
RASH PRURITIC ( 79 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 78 FDA reports)
SHOCK ( 78 FDA reports)
BURSITIS ( 77 FDA reports)
FEELING ABNORMAL ( 77 FDA reports)
LUNG INFILTRATION ( 77 FDA reports)
RENAL IMPAIRMENT ( 77 FDA reports)
BONE DEBRIDEMENT ( 76 FDA reports)
HYPERCHOLESTEROLAEMIA ( 76 FDA reports)
DERMATITIS BULLOUS ( 75 FDA reports)
SPINAL COLUMN STENOSIS ( 75 FDA reports)
URINARY RETENTION ( 75 FDA reports)
EJECTION FRACTION DECREASED ( 74 FDA reports)
GINGIVAL DISORDER ( 74 FDA reports)
HAEMORRHAGE ( 74 FDA reports)
CARDIAC MURMUR ( 73 FDA reports)
CHOLECYSTITIS ( 73 FDA reports)
GOITRE ( 73 FDA reports)
HAEMOPTYSIS ( 73 FDA reports)
HEPATOCELLULAR DAMAGE ( 73 FDA reports)
BLOOD PRESSURE INCREASED ( 72 FDA reports)
DENTAL OPERATION ( 72 FDA reports)
ILEUS ( 72 FDA reports)
OBESITY ( 72 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 71 FDA reports)
CIRCULATORY COLLAPSE ( 71 FDA reports)
CYANOSIS ( 71 FDA reports)
DISEASE PROGRESSION ( 71 FDA reports)
EXCORIATION ( 71 FDA reports)
EYELID OEDEMA ( 71 FDA reports)
HYPERTHERMIA ( 71 FDA reports)
PATHOLOGICAL FRACTURE ( 71 FDA reports)
RESPIRATORY DISORDER ( 71 FDA reports)
BRADYCARDIA ( 70 FDA reports)
DIPLOPIA ( 70 FDA reports)
DYSGEUSIA ( 70 FDA reports)
JAW OPERATION ( 70 FDA reports)
ODYNOPHAGIA ( 70 FDA reports)
PHYSICAL DISABILITY ( 70 FDA reports)
ARRHYTHMIA ( 69 FDA reports)
HAEMATOCRIT DECREASED ( 69 FDA reports)
MASS ( 69 FDA reports)
METABOLIC ACIDOSIS ( 69 FDA reports)
SCAR ( 69 FDA reports)
VISUAL IMPAIRMENT ( 69 FDA reports)
BLOOD CALCIUM DECREASED ( 68 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 68 FDA reports)
FIBROMYALGIA ( 68 FDA reports)
LIFE EXPECTANCY SHORTENED ( 68 FDA reports)
PANCREATITIS ( 68 FDA reports)
PRURITUS GENERALISED ( 68 FDA reports)
ABSCESS ( 67 FDA reports)
AMNESIA ( 67 FDA reports)
COLONIC POLYP ( 67 FDA reports)
FACIAL PAIN ( 67 FDA reports)
HEPATIC CYST ( 67 FDA reports)
PNEUMONIA ASPIRATION ( 67 FDA reports)
RASH MACULAR ( 67 FDA reports)
RHINORRHOEA ( 67 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 67 FDA reports)
BASAL CELL CARCINOMA ( 66 FDA reports)
CHRONIC SINUSITIS ( 66 FDA reports)
GINGIVAL BLEEDING ( 66 FDA reports)
HEPATOCELLULAR INJURY ( 66 FDA reports)
JAW DISORDER ( 66 FDA reports)
ABDOMINAL DISCOMFORT ( 65 FDA reports)
BONE OPERATION ( 65 FDA reports)
ESCHERICHIA INFECTION ( 65 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 65 FDA reports)
JAUNDICE CHOLESTATIC ( 65 FDA reports)
LYMPHOPENIA ( 65 FDA reports)
PRODUCTIVE COUGH ( 65 FDA reports)
CERVICAL SPINAL STENOSIS ( 64 FDA reports)
GINGIVAL PAIN ( 64 FDA reports)
HAEMATEMESIS ( 64 FDA reports)
KYPHOSIS ( 64 FDA reports)
LEFT ATRIAL DILATATION ( 64 FDA reports)
PURULENT DISCHARGE ( 64 FDA reports)
VASCULITIS ( 64 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 63 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 63 FDA reports)
METASTASES TO LUNG ( 63 FDA reports)
OROPHARYNGEAL PAIN ( 63 FDA reports)
STEM CELL TRANSPLANT ( 63 FDA reports)
ULCER ( 63 FDA reports)
FAECES DISCOLOURED ( 62 FDA reports)
TENDONITIS ( 62 FDA reports)
ORTHOSTATIC HYPOTENSION ( 61 FDA reports)
PROTEINURIA ( 61 FDA reports)
SUICIDAL IDEATION ( 61 FDA reports)
TOOTH FRACTURE ( 61 FDA reports)
DYSKINESIA ( 60 FDA reports)
GINGIVAL INFECTION ( 60 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 60 FDA reports)
OSTEOSCLEROSIS ( 60 FDA reports)
PERICARDIAL EFFUSION ( 60 FDA reports)
PERIODONTITIS ( 60 FDA reports)
POLLAKIURIA ( 60 FDA reports)
PULMONARY CONGESTION ( 60 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 59 FDA reports)
ENCEPHALOPATHY ( 59 FDA reports)
EYE PAIN ( 59 FDA reports)
HALLUCINATION ( 59 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 59 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 58 FDA reports)
DENTURE WEARER ( 58 FDA reports)
HEPATOTOXICITY ( 58 FDA reports)
PANCREATITIS ACUTE ( 58 FDA reports)
SENSITIVITY OF TEETH ( 58 FDA reports)
SEQUESTRECTOMY ( 58 FDA reports)
ABDOMINAL HERNIA ( 57 FDA reports)
CROHN'S DISEASE ( 57 FDA reports)
DYSPHONIA ( 57 FDA reports)
IRON DEFICIENCY ANAEMIA ( 57 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 57 FDA reports)
TYPE 2 DIABETES MELLITUS ( 57 FDA reports)
CYST ( 56 FDA reports)
HUMERUS FRACTURE ( 56 FDA reports)
LYMPHOEDEMA ( 56 FDA reports)
METASTASES TO SPINE ( 56 FDA reports)
MYELOMA RECURRENCE ( 56 FDA reports)
CHOLECYSTITIS CHRONIC ( 55 FDA reports)
COAGULOPATHY ( 55 FDA reports)
DRUG ERUPTION ( 55 FDA reports)
FLANK PAIN ( 55 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 55 FDA reports)
MALNUTRITION ( 55 FDA reports)
MENTAL DISORDER ( 55 FDA reports)
NIGHT SWEATS ( 55 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 55 FDA reports)
SQUAMOUS CELL CARCINOMA ( 55 FDA reports)
APHASIA ( 54 FDA reports)
COLITIS ULCERATIVE ( 54 FDA reports)
DRY MOUTH ( 54 FDA reports)
EXPOSED BONE IN JAW ( 54 FDA reports)
GASTROINTESTINAL DISORDER ( 54 FDA reports)
SLEEP DISORDER ( 54 FDA reports)
UTERINE LEIOMYOMA ( 54 FDA reports)
VIRAL INFECTION ( 54 FDA reports)
ATAXIA ( 53 FDA reports)
BLOOD UREA INCREASED ( 53 FDA reports)
BRONCHOPNEUMONIA ( 53 FDA reports)
CONJUNCTIVITIS ( 53 FDA reports)
DEAFNESS ( 53 FDA reports)
DERMATITIS ( 53 FDA reports)
GROIN PAIN ( 53 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 53 FDA reports)
JOINT SWELLING ( 53 FDA reports)
METASTATIC NEOPLASM ( 53 FDA reports)
RASH PAPULAR ( 53 FDA reports)
TONGUE DISCOLOURATION ( 53 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 52 FDA reports)
AORTIC VALVE INCOMPETENCE ( 52 FDA reports)
MOBILITY DECREASED ( 52 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 52 FDA reports)
UNRESPONSIVE TO STIMULI ( 52 FDA reports)
CARDIO-RESPIRATORY ARREST ( 51 FDA reports)
DISTURBANCE IN ATTENTION ( 51 FDA reports)
GALLBLADDER DISORDER ( 51 FDA reports)
NERVOUSNESS ( 51 FDA reports)
PNEUMONITIS ( 51 FDA reports)
ABSCESS JAW ( 50 FDA reports)
AGGRESSION ( 50 FDA reports)
ANURIA ( 50 FDA reports)
COMA ( 50 FDA reports)
DIVERTICULITIS ( 50 FDA reports)
DRY EYE ( 50 FDA reports)
ERYTHEMA MULTIFORME ( 50 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 50 FDA reports)
ORAL CAVITY FISTULA ( 50 FDA reports)
PALLOR ( 50 FDA reports)
BLOOD ALBUMIN DECREASED ( 49 FDA reports)
HIP FRACTURE ( 49 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 49 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 49 FDA reports)
NEOPLASM PROGRESSION ( 49 FDA reports)
PRURIGO ( 49 FDA reports)
RADICULOPATHY ( 49 FDA reports)
RESPIRATORY TRACT INFECTION ( 49 FDA reports)
RHABDOMYOLYSIS ( 49 FDA reports)
SPONDYLOLISTHESIS ( 49 FDA reports)
TOOTH INFECTION ( 49 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 49 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 49 FDA reports)
ACTINOMYCOSIS ( 48 FDA reports)
CARDIOMYOPATHY ( 48 FDA reports)
CHEILITIS ( 48 FDA reports)
DRUG DEPENDENCE ( 48 FDA reports)
GENERALISED OEDEMA ( 48 FDA reports)
INFLUENZA LIKE ILLNESS ( 48 FDA reports)
LOOSE TOOTH ( 48 FDA reports)
PANIC ATTACK ( 48 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 48 FDA reports)
RALES ( 48 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 47 FDA reports)
EATING DISORDER ( 47 FDA reports)
FOOT FRACTURE ( 47 FDA reports)
JOINT DISLOCATION ( 47 FDA reports)
PROTHROMBIN TIME PROLONGED ( 47 FDA reports)
WALKING AID USER ( 47 FDA reports)
BLOOD POTASSIUM DECREASED ( 46 FDA reports)
DECUBITUS ULCER ( 46 FDA reports)
LOCAL SWELLING ( 46 FDA reports)
OTITIS MEDIA ( 46 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 46 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 45 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 45 FDA reports)
DIALYSIS ( 45 FDA reports)
HYPERBILIRUBINAEMIA ( 45 FDA reports)
LIP SWELLING ( 45 FDA reports)
RHEUMATOID ARTHRITIS ( 45 FDA reports)
VISUAL ACUITY REDUCED ( 45 FDA reports)
BACTERAEMIA ( 44 FDA reports)
CYSTITIS ( 44 FDA reports)
ECONOMIC PROBLEM ( 44 FDA reports)
FUNGAL INFECTION ( 44 FDA reports)
HEAD INJURY ( 44 FDA reports)
ROAD TRAFFIC ACCIDENT ( 44 FDA reports)
SYNOVIAL CYST ( 44 FDA reports)
TENDERNESS ( 44 FDA reports)
ABSCESS DRAINAGE ( 43 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 43 FDA reports)
BONE EROSION ( 43 FDA reports)
BURNING SENSATION ( 43 FDA reports)
CLOSTRIDIAL INFECTION ( 43 FDA reports)
DEVICE RELATED INFECTION ( 43 FDA reports)
ENTEROCOCCAL INFECTION ( 43 FDA reports)
INFLUENZA ( 43 FDA reports)
MEDICATION ERROR ( 43 FDA reports)
SINUS CONGESTION ( 43 FDA reports)
THROMBOSIS ( 43 FDA reports)
VENTRICULAR TACHYCARDIA ( 43 FDA reports)
VITREOUS FLOATERS ( 42 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 42 FDA reports)
CARDIOVASCULAR DISORDER ( 42 FDA reports)
CAROTID ARTERY STENOSIS ( 42 FDA reports)
DERMATITIS ALLERGIC ( 42 FDA reports)
EAR INFECTION ( 42 FDA reports)
HYDRONEPHROSIS ( 42 FDA reports)
PNEUMOTHORAX ( 42 FDA reports)
PRESYNCOPE ( 42 FDA reports)
PULMONARY FIBROSIS ( 42 FDA reports)
RESPIRATORY ARREST ( 42 FDA reports)
STRESS ( 42 FDA reports)
ACUTE RESPIRATORY FAILURE ( 41 FDA reports)
FOOT DEFORMITY ( 41 FDA reports)
LACERATION ( 41 FDA reports)
LUNG CONSOLIDATION ( 41 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 41 FDA reports)
MYOCARDIAL ISCHAEMIA ( 41 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 41 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 41 FDA reports)
CRYING ( 40 FDA reports)
DELIRIUM ( 40 FDA reports)
HYPOTHYROIDISM ( 40 FDA reports)
LUNG NEOPLASM MALIGNANT ( 40 FDA reports)
MUSCLE TWITCHING ( 40 FDA reports)
NEUTROPHIL COUNT INCREASED ( 40 FDA reports)
PROSTATOMEGALY ( 40 FDA reports)
THROMBOCYTOSIS ( 40 FDA reports)
BLOOD GLUCOSE DECREASED ( 39 FDA reports)
BONE FRAGMENTATION ( 39 FDA reports)
BRUXISM ( 39 FDA reports)
GASTRIC POLYPS ( 39 FDA reports)
GASTRIC ULCER ( 39 FDA reports)
GINGIVAL RECESSION ( 39 FDA reports)
HEPATIC LESION ( 39 FDA reports)
NECK MASS ( 39 FDA reports)
SWOLLEN TONGUE ( 39 FDA reports)
ABNORMAL BEHAVIOUR ( 38 FDA reports)
ANGIONEUROTIC OEDEMA ( 38 FDA reports)
APPENDICECTOMY ( 38 FDA reports)
APPENDICITIS ( 38 FDA reports)
BONE MARROW TRANSPLANT ( 38 FDA reports)
CARDIOGENIC SHOCK ( 38 FDA reports)
DYSARTHRIA ( 38 FDA reports)
ECCHYMOSIS ( 38 FDA reports)
EOSINOPHIL COUNT INCREASED ( 38 FDA reports)
HILAR LYMPHADENOPATHY ( 38 FDA reports)
LOBAR PNEUMONIA ( 38 FDA reports)
PETECHIAE ( 38 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 38 FDA reports)
SPEECH DISORDER ( 38 FDA reports)
SPINAL CORD COMPRESSION ( 38 FDA reports)
TOOTH INJURY ( 38 FDA reports)
WOUND INFECTION ( 38 FDA reports)
ABSCESS ORAL ( 37 FDA reports)
ADRENAL INSUFFICIENCY ( 37 FDA reports)
ANGINA UNSTABLE ( 37 FDA reports)
BODY TEMPERATURE INCREASED ( 37 FDA reports)
BONE DENSITY DECREASED ( 37 FDA reports)
CEREBRAL ISCHAEMIA ( 37 FDA reports)
CHOLANGITIS ( 37 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 37 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 37 FDA reports)
GLOSSODYNIA ( 37 FDA reports)
MYOCLONUS ( 37 FDA reports)
NEUTROPHIL COUNT DECREASED ( 37 FDA reports)
SCIATICA ( 37 FDA reports)
VAGINAL HAEMORRHAGE ( 37 FDA reports)
DERMATITIS CONTACT ( 36 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 36 FDA reports)
FLUSHING ( 36 FDA reports)
GASTROENTERITIS ( 36 FDA reports)
HYPERKERATOSIS ( 36 FDA reports)
HYPOALBUMINAEMIA ( 36 FDA reports)
INTESTINAL OBSTRUCTION ( 36 FDA reports)
LIPASE INCREASED ( 36 FDA reports)
PHARYNGITIS ( 36 FDA reports)
RASH MORBILLIFORM ( 36 FDA reports)
RESTLESS LEGS SYNDROME ( 36 FDA reports)
SPLENOMEGALY ( 36 FDA reports)
APNOEA ( 35 FDA reports)
ATRIAL SEPTAL DEFECT ( 35 FDA reports)
CEREBRAL ATROPHY ( 35 FDA reports)
CEREBRAL INFARCTION ( 35 FDA reports)
CHONDROMALACIA ( 35 FDA reports)
DENTAL FISTULA ( 35 FDA reports)
DIVERTICULUM INTESTINAL ( 35 FDA reports)
FAECAL INCONTINENCE ( 35 FDA reports)
FLUID RETENTION ( 35 FDA reports)
HALLUCINATION, VISUAL ( 35 FDA reports)
HYPERCALCAEMIA ( 35 FDA reports)
IRRITABILITY ( 35 FDA reports)
LIP OEDEMA ( 35 FDA reports)
LUNG INFECTION ( 35 FDA reports)
ORAL SURGERY ( 35 FDA reports)
PLATELET COUNT INCREASED ( 35 FDA reports)
SKIN DISCOLOURATION ( 35 FDA reports)
TONGUE INJURY ( 35 FDA reports)
VENOUS THROMBOSIS ( 35 FDA reports)
ANIMAL BITE ( 34 FDA reports)
CAESAREAN SECTION ( 34 FDA reports)
DEVICE FAILURE ( 34 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 34 FDA reports)
FEAR ( 34 FDA reports)
FEELING HOT ( 34 FDA reports)
FLATULENCE ( 34 FDA reports)
GINGIVAL ULCERATION ( 34 FDA reports)
GLAUCOMA ( 34 FDA reports)
LACRIMATION INCREASED ( 34 FDA reports)
RESTLESSNESS ( 34 FDA reports)
ASPIRATION PLEURAL CAVITY ( 33 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 33 FDA reports)
BLOOD POTASSIUM INCREASED ( 33 FDA reports)
BRONCHIECTASIS ( 33 FDA reports)
DRY SKIN ( 33 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 33 FDA reports)
GRANULOMA ( 33 FDA reports)
HAEMANGIOMA ( 33 FDA reports)
ILL-DEFINED DISORDER ( 33 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 33 FDA reports)
NEPHRITIS INTERSTITIAL ( 33 FDA reports)
PHARYNGEAL OEDEMA ( 33 FDA reports)
ABASIA ( 32 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 32 FDA reports)
BACK INJURY ( 32 FDA reports)
BREATH ODOUR ( 32 FDA reports)
GRANULOCYTOPENIA ( 32 FDA reports)
HYPOACUSIS ( 32 FDA reports)
LABORATORY TEST ABNORMAL ( 32 FDA reports)
LUMBAR RADICULOPATHY ( 32 FDA reports)
METASTASES TO LIVER ( 32 FDA reports)
NASAL SEPTUM DEVIATION ( 32 FDA reports)
OSTEOMYELITIS CHRONIC ( 32 FDA reports)
PELVIC PAIN ( 32 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 32 FDA reports)
ACTINIC KERATOSIS ( 31 FDA reports)
AZOTAEMIA ( 31 FDA reports)
BONE NEOPLASM ( 31 FDA reports)
COLON ADENOMA ( 31 FDA reports)
HAEMOLYTIC ANAEMIA ( 31 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 31 FDA reports)
LETHARGY ( 31 FDA reports)
LOCALISED INFECTION ( 31 FDA reports)
MUSCLE STRAIN ( 31 FDA reports)
OSTEITIS DEFORMANS ( 31 FDA reports)
SINUS ARRHYTHMIA ( 31 FDA reports)
SKIN BURNING SENSATION ( 31 FDA reports)
SPINAL DISORDER ( 31 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 31 FDA reports)
ABSCESS NECK ( 30 FDA reports)
BLOOD SODIUM DECREASED ( 30 FDA reports)
CERVICOBRACHIAL SYNDROME ( 30 FDA reports)
HAEMOLYSIS ( 30 FDA reports)
LARYNGEAL OEDEMA ( 30 FDA reports)
LIVER INJURY ( 30 FDA reports)
MIXED LIVER INJURY ( 30 FDA reports)
NEURODERMATITIS ( 30 FDA reports)
NOCTURIA ( 30 FDA reports)
OCULAR ICTERUS ( 30 FDA reports)
ORTHOPNOEA ( 30 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 30 FDA reports)
PELVIC FRACTURE ( 30 FDA reports)
RHINITIS ALLERGIC ( 30 FDA reports)
SUDDEN DEATH ( 30 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 30 FDA reports)
UTERINE HAEMORRHAGE ( 30 FDA reports)
CATARACT OPERATION ( 29 FDA reports)
DILATATION VENTRICULAR ( 29 FDA reports)
EDENTULOUS ( 29 FDA reports)
FAILURE TO THRIVE ( 29 FDA reports)
HAEMODIALYSIS ( 29 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 29 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 29 FDA reports)
LIMB INJURY ( 29 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 29 FDA reports)
MENORRHAGIA ( 29 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 29 FDA reports)
PLANTAR FASCIITIS ( 29 FDA reports)
PSEUDOMONAS INFECTION ( 29 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 29 FDA reports)
SUICIDE ATTEMPT ( 29 FDA reports)
TACHYPNOEA ( 29 FDA reports)
TINNITUS ( 29 FDA reports)
ABDOMINAL PAIN LOWER ( 28 FDA reports)
ACROCHORDON ( 28 FDA reports)
ALVEOLOPLASTY ( 28 FDA reports)
AORTIC ANEURYSM ( 28 FDA reports)
BLEPHARITIS ( 28 FDA reports)
BONE LOSS ( 28 FDA reports)
CHOLECYSTITIS ACUTE ( 28 FDA reports)
DEMENTIA ( 28 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 28 FDA reports)
FRACTURED SACRUM ( 28 FDA reports)
GINGIVAL EROSION ( 28 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 28 FDA reports)
MENISCUS LESION ( 28 FDA reports)
NASOPHARYNGITIS ( 28 FDA reports)
NEPHROPATHY ( 28 FDA reports)
PAINFUL RESPIRATION ( 28 FDA reports)
RESPIRATORY TRACT CONGESTION ( 28 FDA reports)
UPPER LIMB FRACTURE ( 28 FDA reports)
ACUTE CORONARY SYNDROME ( 27 FDA reports)
CARDIAC VALVE DISEASE ( 27 FDA reports)
EMPYEMA ( 27 FDA reports)
EPILEPSY ( 27 FDA reports)
GINGIVAL ERYTHEMA ( 27 FDA reports)
HEPATITIS ACUTE ( 27 FDA reports)
INCORRECT DOSE ADMINISTERED ( 27 FDA reports)
INGUINAL HERNIA ( 27 FDA reports)
MOUTH HAEMORRHAGE ( 27 FDA reports)
VARICES OESOPHAGEAL ( 27 FDA reports)
WOUND ( 27 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 26 FDA reports)
BLOOD URINE PRESENT ( 26 FDA reports)
BONE NEOPLASM MALIGNANT ( 26 FDA reports)
COLON CANCER ( 26 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 26 FDA reports)
DIABETIC RETINOPATHY ( 26 FDA reports)
ESSENTIAL HYPERTENSION ( 26 FDA reports)
GOUT ( 26 FDA reports)
HYPOAESTHESIA ORAL ( 26 FDA reports)
JOINT STIFFNESS ( 26 FDA reports)
MITRAL VALVE CALCIFICATION ( 26 FDA reports)
NERVOUS SYSTEM DISORDER ( 26 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 26 FDA reports)
PHLEBITIS ( 26 FDA reports)
POST PROCEDURAL COMPLICATION ( 26 FDA reports)
PRESBYOPIA ( 26 FDA reports)
PULPITIS DENTAL ( 26 FDA reports)
RENAL TUBULAR NECROSIS ( 26 FDA reports)
SKIN LACERATION ( 26 FDA reports)
SPUTUM DISCOLOURED ( 26 FDA reports)
ACUTE PULMONARY OEDEMA ( 25 FDA reports)
BUNION ( 25 FDA reports)
CLOSTRIDIUM COLITIS ( 25 FDA reports)
DEAFNESS NEUROSENSORY ( 25 FDA reports)
DENTAL DISCOMFORT ( 25 FDA reports)
DEPRESSED MOOD ( 25 FDA reports)
DRUG TOXICITY ( 25 FDA reports)
DYSAESTHESIA ( 25 FDA reports)
HAEMODYNAMIC INSTABILITY ( 25 FDA reports)
HEPATIC MASS ( 25 FDA reports)
HEPATIC PAIN ( 25 FDA reports)
JUGULAR VEIN THROMBOSIS ( 25 FDA reports)
LABYRINTHITIS ( 25 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 25 FDA reports)
NEOPLASM ( 25 FDA reports)
NIKOLSKY'S SIGN ( 25 FDA reports)
NODULE ( 25 FDA reports)
OEDEMA MOUTH ( 25 FDA reports)
OFF LABEL USE ( 25 FDA reports)
OTITIS EXTERNA ( 25 FDA reports)
OVARIAN CYST ( 25 FDA reports)
PERONEAL NERVE PALSY ( 25 FDA reports)
POLYP ( 25 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 25 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 25 FDA reports)
SEDATION ( 25 FDA reports)
SPINAL LAMINECTOMY ( 25 FDA reports)
SUBCUTANEOUS NODULE ( 25 FDA reports)
SURGERY ( 25 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 25 FDA reports)
TRISMUS ( 25 FDA reports)
WEGENER'S GRANULOMATOSIS ( 25 FDA reports)
VASCULAR PURPURA ( 24 FDA reports)
VENTRICULAR HYPERTROPHY ( 24 FDA reports)
VIITH NERVE PARALYSIS ( 24 FDA reports)
ABNORMAL FAECES ( 24 FDA reports)
ANAPHYLACTOID REACTION ( 24 FDA reports)
DRUG ABUSE ( 24 FDA reports)
EMOTIONAL DISORDER ( 24 FDA reports)
HYPOPHOSPHATAEMIA ( 24 FDA reports)
HYPOVENTILATION ( 24 FDA reports)
ISCHAEMIA ( 24 FDA reports)
JOINT SPRAIN ( 24 FDA reports)
LYMPHOMA ( 24 FDA reports)
MYOPIA ( 24 FDA reports)
PEPTIC ULCER ( 24 FDA reports)
PLEURAL FIBROSIS ( 24 FDA reports)
SINUS BRADYCARDIA ( 24 FDA reports)
TARDIVE DYSKINESIA ( 24 FDA reports)
UROSEPSIS ( 24 FDA reports)
ALVEOLITIS ( 23 FDA reports)
ANGER ( 23 FDA reports)
APTYALISM ( 23 FDA reports)
BODY TEMPERATURE DECREASED ( 23 FDA reports)
COLD SWEAT ( 23 FDA reports)
DEVELOPMENTAL DELAY ( 23 FDA reports)
DYSLIPIDAEMIA ( 23 FDA reports)
DYSTONIA ( 23 FDA reports)
GRAND MAL CONVULSION ( 23 FDA reports)
HIP ARTHROPLASTY ( 23 FDA reports)
HODGKIN'S DISEASE ( 23 FDA reports)
LUDWIG ANGINA ( 23 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 23 FDA reports)
MAJOR DEPRESSION ( 23 FDA reports)
MEMORY IMPAIRMENT ( 23 FDA reports)
MICTURITION URGENCY ( 23 FDA reports)
MYELOPATHY ( 23 FDA reports)
NEURITIS ( 23 FDA reports)
OESOPHAGITIS ULCERATIVE ( 23 FDA reports)
PALATAL OEDEMA ( 23 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 23 FDA reports)
RETINOPATHY ( 23 FDA reports)
SCLERODERMA ( 23 FDA reports)
SKIN PAPILLOMA ( 23 FDA reports)
SOFT TISSUE DISORDER ( 23 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 23 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
TONGUE OEDEMA ( 23 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 23 FDA reports)
ABSCESS LIMB ( 22 FDA reports)
ACIDOSIS ( 22 FDA reports)
AORTIC DILATATION ( 22 FDA reports)
BLINDNESS ( 22 FDA reports)
BONE SCAN ABNORMAL ( 22 FDA reports)
BRONCHITIS CHRONIC ( 22 FDA reports)
DIASTOLIC DYSFUNCTION ( 22 FDA reports)
EAR DISCOMFORT ( 22 FDA reports)
ENTERITIS ( 22 FDA reports)
FRACTURE ( 22 FDA reports)
GASTRODUODENITIS ( 22 FDA reports)
GENERALISED ANXIETY DISORDER ( 22 FDA reports)
HEPATIC NECROSIS ( 22 FDA reports)
HYPERPARATHYROIDISM ( 22 FDA reports)
JOINT EFFUSION ( 22 FDA reports)
KIDNEY INFECTION ( 22 FDA reports)
LACTIC ACIDOSIS ( 22 FDA reports)
MITRAL VALVE PROLAPSE ( 22 FDA reports)
MOOD SWINGS ( 22 FDA reports)
ORAL FUNGAL INFECTION ( 22 FDA reports)
ORAL HERPES ( 22 FDA reports)
OSTEORADIONECROSIS ( 22 FDA reports)
PLEURISY ( 22 FDA reports)
POOR QUALITY SLEEP ( 22 FDA reports)
PSYCHOTIC DISORDER ( 22 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 22 FDA reports)
SENSORY DISTURBANCE ( 22 FDA reports)
SKIN NECROSIS ( 22 FDA reports)
SPINAL FRACTURE ( 22 FDA reports)
SUBDURAL HAEMATOMA ( 22 FDA reports)
TREATMENT NONCOMPLIANCE ( 22 FDA reports)
UNEVALUABLE EVENT ( 22 FDA reports)
URGE INCONTINENCE ( 22 FDA reports)
VITAMIN B12 DEFICIENCY ( 22 FDA reports)
VITREOUS DETACHMENT ( 22 FDA reports)
WITHDRAWAL SYNDROME ( 21 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 21 FDA reports)
ACUTE HEPATIC FAILURE ( 21 FDA reports)
ADENOMYOSIS ( 21 FDA reports)
ADVERSE DRUG REACTION ( 21 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 21 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 21 FDA reports)
CHOLECYSTECTOMY ( 21 FDA reports)
DRUG INTOLERANCE ( 21 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 21 FDA reports)
FACIAL NEURALGIA ( 21 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 21 FDA reports)
GASTROINTESTINAL PAIN ( 21 FDA reports)
HEPATITIS TOXIC ( 21 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 21 FDA reports)
MACULOPATHY ( 21 FDA reports)
MALOCCLUSION ( 21 FDA reports)
MECHANICAL VENTILATION ( 21 FDA reports)
MELANOCYTIC NAEVUS ( 21 FDA reports)
MUSCLE DISORDER ( 21 FDA reports)
MYOPATHY ( 21 FDA reports)
NEUROLOGICAL SYMPTOM ( 21 FDA reports)
OROANTRAL FISTULA ( 21 FDA reports)
PARAESTHESIA ORAL ( 21 FDA reports)
PLASMACYTOMA ( 21 FDA reports)
POOR DENTAL CONDITION ( 21 FDA reports)
RENAL DISORDER ( 21 FDA reports)
SKIN TEST POSITIVE ( 21 FDA reports)
TENDON DISORDER ( 21 FDA reports)
ANKLE FRACTURE ( 20 FDA reports)
APHTHOUS STOMATITIS ( 20 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 20 FDA reports)
ATRIAL FLUTTER ( 20 FDA reports)
BREATH SOUNDS ABNORMAL ( 20 FDA reports)
CHOLESTATIC LIVER INJURY ( 20 FDA reports)
EROSIVE OESOPHAGITIS ( 20 FDA reports)
FRACTURE NONUNION ( 20 FDA reports)
GYNAECOMASTIA ( 20 FDA reports)
HYPOTHERMIA ( 20 FDA reports)
HYPOVOLAEMIC SHOCK ( 20 FDA reports)
IRRITABLE BOWEL SYNDROME ( 20 FDA reports)
KLEBSIELLA INFECTION ( 20 FDA reports)
LEUKAEMIA ( 20 FDA reports)
MUCOUS MEMBRANE DISORDER ( 20 FDA reports)
MYASTHENIA GRAVIS ( 20 FDA reports)
NEUTROPENIC SEPSIS ( 20 FDA reports)
OEDEMA MUCOSAL ( 20 FDA reports)
PARALYSIS ( 20 FDA reports)
PERITONEAL EFFUSION ( 20 FDA reports)
PHOTOSENSITIVITY REACTION ( 20 FDA reports)
PROSTATE CANCER ( 20 FDA reports)
PURULENCE ( 20 FDA reports)
RADIATION SKIN INJURY ( 20 FDA reports)
RESPIRATORY ACIDOSIS ( 20 FDA reports)
SCAB ( 20 FDA reports)
TEMPERATURE INTOLERANCE ( 20 FDA reports)
THERMAL BURN ( 20 FDA reports)
TRYPTASE INCREASED ( 20 FDA reports)
VENOUS INSUFFICIENCY ( 20 FDA reports)
VENOUS THROMBOSIS LIMB ( 20 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 20 FDA reports)
X-RAY ABNORMAL ( 20 FDA reports)
VASCULAR CALCIFICATION ( 19 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 19 FDA reports)
BACK DISORDER ( 19 FDA reports)
BONE CALLUS EXCESSIVE ( 19 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 19 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 19 FDA reports)
DEVICE MALFUNCTION ( 19 FDA reports)
DISEASE RECURRENCE ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 19 FDA reports)
EXOPHTHALMOS ( 19 FDA reports)
FLUID OVERLOAD ( 19 FDA reports)
GASTRIC DISORDER ( 19 FDA reports)
HEPATIC CIRRHOSIS ( 19 FDA reports)
HYPERTHYROIDISM ( 19 FDA reports)
HYPOMAGNESAEMIA ( 19 FDA reports)
LEFT VENTRICULAR FAILURE ( 19 FDA reports)
LIPOMA ( 19 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 19 FDA reports)
MYELODYSPLASTIC SYNDROME ( 19 FDA reports)
ONYCHOMYCOSIS ( 19 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 19 FDA reports)
POST PROCEDURAL FISTULA ( 19 FDA reports)
PSORIASIS ( 19 FDA reports)
PULSE ABSENT ( 19 FDA reports)
QUADRIPLEGIA ( 19 FDA reports)
RENAL PAIN ( 19 FDA reports)
RHINITIS ( 19 FDA reports)
SKIN EROSION ( 19 FDA reports)
SKIN REACTION ( 19 FDA reports)
SPONDYLOLYSIS ( 19 FDA reports)
THYROID NEOPLASM ( 19 FDA reports)
TOOTH IMPACTED ( 19 FDA reports)
TOOTH REPAIR ( 19 FDA reports)
URTICARIA GENERALISED ( 19 FDA reports)
ATROPHIC VULVOVAGINITIS ( 18 FDA reports)
AUTOIMMUNE HEPATITIS ( 18 FDA reports)
BREAST CANCER METASTATIC ( 18 FDA reports)
BREAST OPERATION ( 18 FDA reports)
BRONCHIAL SECRETION RETENTION ( 18 FDA reports)
CATHETER PLACEMENT ( 18 FDA reports)
CEREBRAL HAEMORRHAGE ( 18 FDA reports)
COCCYDYNIA ( 18 FDA reports)
CRANIAL NERVE DISORDER ( 18 FDA reports)
DILATATION ATRIAL ( 18 FDA reports)
DUODENITIS ( 18 FDA reports)
ELECTROLYTE IMBALANCE ( 18 FDA reports)
EOSINOPHIL COUNT DECREASED ( 18 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 18 FDA reports)
EYE DISORDER ( 18 FDA reports)
FEBRILE BONE MARROW APLASIA ( 18 FDA reports)
GRAFT VERSUS HOST DISEASE ( 18 FDA reports)
HEART RATE IRREGULAR ( 18 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 18 FDA reports)
HEPATIC ENCEPHALOPATHY ( 18 FDA reports)
HYPERPLASIA ( 18 FDA reports)
INGROWING NAIL ( 18 FDA reports)
LEG AMPUTATION ( 18 FDA reports)
LIGAMENT SPRAIN ( 18 FDA reports)
MICROCYTIC ANAEMIA ( 18 FDA reports)
MULTIPLE INJURIES ( 18 FDA reports)
MULTIPLE SCLEROSIS ( 18 FDA reports)
NEPHROTIC SYNDROME ( 18 FDA reports)
OESOPHAGEAL STENOSIS ( 18 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 18 FDA reports)
PROTHROMBIN TIME SHORTENED ( 18 FDA reports)
PYELONEPHRITIS ( 18 FDA reports)
RASH SCARLATINIFORM ( 18 FDA reports)
SARCOIDOSIS ( 18 FDA reports)
SKIN HYPERPIGMENTATION ( 18 FDA reports)
SPLENIC LESION ( 18 FDA reports)
THROAT TIGHTNESS ( 18 FDA reports)
URETEROSTOMY SITE DISCOMFORT ( 18 FDA reports)
VARICOSE VEIN ( 18 FDA reports)
VISUAL DISTURBANCE ( 18 FDA reports)
WOUND HAEMORRHAGE ( 18 FDA reports)
VASCULAR PSEUDOANEURYSM ( 17 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 17 FDA reports)
VENOUS OCCLUSION ( 17 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
ACCOMMODATION DISORDER ( 17 FDA reports)
ADVERSE EVENT ( 17 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 17 FDA reports)
AMBLYOPIA ( 17 FDA reports)
AORTIC CALCIFICATION ( 17 FDA reports)
BIOPSY BONE MARROW ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 17 FDA reports)
BREAST PAIN ( 17 FDA reports)
CERVICAL CORD COMPRESSION ( 17 FDA reports)
DENTAL PLAQUE ( 17 FDA reports)
DENTAL PULP DISORDER ( 17 FDA reports)
DRUG ADMINISTRATION ERROR ( 17 FDA reports)
EAR HAEMORRHAGE ( 17 FDA reports)
EMBOLISM ( 17 FDA reports)
ERYSIPELAS ( 17 FDA reports)
EYE IRRITATION ( 17 FDA reports)
FEMUR FRACTURE ( 17 FDA reports)
FIBROSIS ( 17 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 17 FDA reports)
HEPATOSPLENOMEGALY ( 17 FDA reports)
HYPOGONADISM ( 17 FDA reports)
HYPOTONIA ( 17 FDA reports)
ILEITIS ( 17 FDA reports)
IMMUNOSUPPRESSION ( 17 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 17 FDA reports)
INTESTINAL PERFORATION ( 17 FDA reports)
JOINT INJURY ( 17 FDA reports)
LEUKOENCEPHALOPATHY ( 17 FDA reports)
LIBIDO DECREASED ( 17 FDA reports)
METASTASES TO LYMPH NODES ( 17 FDA reports)
MUSCLE HAEMORRHAGE ( 17 FDA reports)
OPEN REDUCTION OF FRACTURE ( 17 FDA reports)
PAIN OF SKIN ( 17 FDA reports)
PERFORMANCE STATUS DECREASED ( 17 FDA reports)
POLYARTHRITIS ( 17 FDA reports)
PROTEIN URINE PRESENT ( 17 FDA reports)
PULMONARY MASS ( 17 FDA reports)
PYOTHORAX ( 17 FDA reports)
RECTAL POLYP ( 17 FDA reports)
SENSORY LOSS ( 17 FDA reports)
SEPSIS SYNDROME ( 17 FDA reports)
SINUS HEADACHE ( 17 FDA reports)
SPINAL FUSION ACQUIRED ( 17 FDA reports)
URETERAL DISORDER ( 17 FDA reports)
ACUTE SINUSITIS ( 16 FDA reports)
BACTERIAL INFECTION ( 16 FDA reports)
BILIARY DILATATION ( 16 FDA reports)
BILIARY DYSKINESIA ( 16 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 16 FDA reports)
BRADYPHRENIA ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
CHEST X-RAY ABNORMAL ( 16 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 16 FDA reports)
CONNECTIVE TISSUE DISORDER ( 16 FDA reports)
COR PULMONALE CHRONIC ( 16 FDA reports)
CORONARY ARTERY STENOSIS ( 16 FDA reports)
DYSSTASIA ( 16 FDA reports)
EXFOLIATIVE RASH ( 16 FDA reports)
FAECES PALE ( 16 FDA reports)
FUNGAL SEPSIS ( 16 FDA reports)
GASTRIC HAEMORRHAGE ( 16 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 16 FDA reports)
HEART RATE DECREASED ( 16 FDA reports)
HYDROCELE ( 16 FDA reports)
HYPOCALCAEMIA ( 16 FDA reports)
HYPOVOLAEMIA ( 16 FDA reports)
INFECTED SKIN ULCER ( 16 FDA reports)
INTENTIONAL OVERDOSE ( 16 FDA reports)
INTESTINAL HAEMORRHAGE ( 16 FDA reports)
KERATITIS ( 16 FDA reports)
LEUKOPLAKIA ORAL ( 16 FDA reports)
MENINGITIS ( 16 FDA reports)
MOVEMENT DISORDER ( 16 FDA reports)
MYOSITIS ( 16 FDA reports)
NEUTROPHILIA ( 16 FDA reports)
OTITIS MEDIA CHRONIC ( 16 FDA reports)
PAPILLOEDEMA ( 16 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 16 FDA reports)
PERITONITIS ( 16 FDA reports)
PORTAL HYPERTENSION ( 16 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 16 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 16 FDA reports)
PYELONEPHRITIS ACUTE ( 16 FDA reports)
RASH VESICULAR ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
SKIN IRRITATION ( 16 FDA reports)
SKIN OEDEMA ( 16 FDA reports)
SUPERINFECTION ( 16 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 16 FDA reports)
THROAT IRRITATION ( 16 FDA reports)
THYROID DISORDER ( 16 FDA reports)
ADRENAL NEOPLASM ( 15 FDA reports)
ANOGENITAL WARTS ( 15 FDA reports)
ANOSMIA ( 15 FDA reports)
AORTIC STENOSIS ( 15 FDA reports)
AORTIC VALVE SCLEROSIS ( 15 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 15 FDA reports)
ASTIGMATISM ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK ( 15 FDA reports)
BLOOD SODIUM INCREASED ( 15 FDA reports)
BRONCHITIS ACUTE ( 15 FDA reports)
CATHETERISATION CARDIAC ( 15 FDA reports)
COGNITIVE DISORDER ( 15 FDA reports)
CONJUNCTIVITIS VIRAL ( 15 FDA reports)
COSTOCHONDRITIS ( 15 FDA reports)
DENTAL PROSTHESIS USER ( 15 FDA reports)
DERMAL CYST ( 15 FDA reports)
EYE LASER SURGERY ( 15 FDA reports)
FISTULA REPAIR ( 15 FDA reports)
GINGIVAL ABSCESS ( 15 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 15 FDA reports)
HEPATIC FIBROSIS ( 15 FDA reports)
HEPATIC NEOPLASM ( 15 FDA reports)
HEPATITIS C ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
INJECTION SITE ERYTHEMA ( 15 FDA reports)
LARYNGITIS ( 15 FDA reports)
LARYNGOSPASM ( 15 FDA reports)
LIP DISORDER ( 15 FDA reports)
LOCALISED OEDEMA ( 15 FDA reports)
MALIGNANT MELANOMA ( 15 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 15 FDA reports)
MONOPARESIS ( 15 FDA reports)
NEURODEGENERATIVE DISORDER ( 15 FDA reports)
OCULAR HYPERTENSION ( 15 FDA reports)
OESOPHAGEAL ULCER ( 15 FDA reports)
ORAL PUSTULE ( 15 FDA reports)
OVERWEIGHT ( 15 FDA reports)
PERIPHERAL ISCHAEMIA ( 15 FDA reports)
POLYURIA ( 15 FDA reports)
PREMATURE BABY ( 15 FDA reports)
RADIUS FRACTURE ( 15 FDA reports)
RENAL INJURY ( 15 FDA reports)
SERUM SICKNESS ( 15 FDA reports)
SHOCK HAEMORRHAGIC ( 15 FDA reports)
SOFT TISSUE INFECTION ( 15 FDA reports)
SOFT TISSUE INFLAMMATION ( 15 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 15 FDA reports)
TROPONIN INCREASED ( 15 FDA reports)
UTERINE ENLARGEMENT ( 15 FDA reports)
WOUND DRAINAGE ( 15 FDA reports)
YELLOW SKIN ( 14 FDA reports)
ABDOMINAL ABSCESS ( 14 FDA reports)
ABORTION SPONTANEOUS ( 14 FDA reports)
ACNE ( 14 FDA reports)
AFFECTIVE DISORDER ( 14 FDA reports)
BLOOD AMYLASE INCREASED ( 14 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 14 FDA reports)
BRAIN MASS ( 14 FDA reports)
BREAST RECONSTRUCTION ( 14 FDA reports)
CHEMICAL POISONING ( 14 FDA reports)
CHONDROCALCINOSIS ( 14 FDA reports)
CUBITAL TUNNEL SYNDROME ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
DIABETIC KETOACIDOSIS ( 14 FDA reports)
DIFFICULTY IN WALKING ( 14 FDA reports)
DYSGRAPHIA ( 14 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 14 FDA reports)
EXTREMITY NECROSIS ( 14 FDA reports)
EYE SWELLING ( 14 FDA reports)
HAEMANGIOMA OF LIVER ( 14 FDA reports)
HERPES SIMPLEX ( 14 FDA reports)
HYPERNATRAEMIA ( 14 FDA reports)
ILEUS PARALYTIC ( 14 FDA reports)
INCONTINENCE ( 14 FDA reports)
LYMPHADENECTOMY ( 14 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
MONOCLONAL GAMMOPATHY ( 14 FDA reports)
MUCOSAL EROSION ( 14 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 14 FDA reports)
OCULAR HYPERAEMIA ( 14 FDA reports)
ORAL DISCOMFORT ( 14 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 14 FDA reports)
ORAL PRURITUS ( 14 FDA reports)
OXYGEN SUPPLEMENTATION ( 14 FDA reports)
PALATAL DISORDER ( 14 FDA reports)
PARAPLEGIA ( 14 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 14 FDA reports)
PNEUMONIA BACTERIAL ( 14 FDA reports)
PROSTHESIS USER ( 14 FDA reports)
PSYCHOMOTOR RETARDATION ( 14 FDA reports)
RADIOTHERAPY ( 14 FDA reports)
RETROPERITONEAL HAEMATOMA ( 14 FDA reports)
SNEEZING ( 14 FDA reports)
SPINAL FUSION SURGERY ( 14 FDA reports)
SUBCUTANEOUS ABSCESS ( 14 FDA reports)
TENOSYNOVITIS ( 14 FDA reports)
ACUTE LEUKAEMIA ( 13 FDA reports)
ANAL ULCER ( 13 FDA reports)
ASPIRATION ( 13 FDA reports)
BARRETT'S OESOPHAGUS ( 13 FDA reports)
BILE DUCT OBSTRUCTION ( 13 FDA reports)
BIOPSY BONE ABNORMAL ( 13 FDA reports)
BLOOD CULTURE POSITIVE ( 13 FDA reports)
BONE GRAFT ( 13 FDA reports)
CACHEXIA ( 13 FDA reports)
CARDIOTOXICITY ( 13 FDA reports)
DIABETIC NEUROPATHY ( 13 FDA reports)
EROSIVE DUODENITIS ( 13 FDA reports)
EYE HAEMORRHAGE ( 13 FDA reports)
FAT TISSUE INCREASED ( 13 FDA reports)
HEPATITIS FULMINANT ( 13 FDA reports)
HYPERCAPNIA ( 13 FDA reports)
HYPERTROPHY ( 13 FDA reports)
LACTOSE INTOLERANCE ( 13 FDA reports)
LARGE INTESTINE PERFORATION ( 13 FDA reports)
LYMPHOCYTOSIS ( 13 FDA reports)
MACULAR DEGENERATION ( 13 FDA reports)
METASTASES TO PERITONEUM ( 13 FDA reports)
METASTASIS ( 13 FDA reports)
MONOCYTE COUNT DECREASED ( 13 FDA reports)
MULTIPLE FRACTURES ( 13 FDA reports)
NERVE ROOT LESION ( 13 FDA reports)
PELVIC ABSCESS ( 13 FDA reports)
PLASMACYTOSIS ( 13 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
PROSTATE CANCER METASTATIC ( 13 FDA reports)
RADIATION OESOPHAGITIS ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
SCAN BONE MARROW ABNORMAL ( 13 FDA reports)
SEBORRHOEIC KERATOSIS ( 13 FDA reports)
SKIN CANCER ( 13 FDA reports)
SNORING ( 13 FDA reports)
SPINAL CORD OEDEMA ( 13 FDA reports)
STREPTOCOCCAL INFECTION ( 13 FDA reports)
STRESS FRACTURE ( 13 FDA reports)
THROMBOCYTHAEMIA ( 13 FDA reports)
TUMOUR HAEMORRHAGE ( 13 FDA reports)
VERTEBROPLASTY ( 13 FDA reports)
VOMITING PROJECTILE ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
WOUND COMPLICATION ( 13 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
ABDOMINAL TENDERNESS ( 12 FDA reports)
ADENOMA BENIGN ( 12 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 12 FDA reports)
ADRENAL DISORDER ( 12 FDA reports)
AMENORRHOEA ( 12 FDA reports)
ANASTOMOTIC LEAK ( 12 FDA reports)
ANXIETY DISORDER ( 12 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
ASPERGILLOSIS ( 12 FDA reports)
AUTISM ( 12 FDA reports)
BACTERIA STOOL IDENTIFIED ( 12 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 12 FDA reports)
BILE DUCT STONE ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 12 FDA reports)
BLOOD IRON DECREASED ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 12 FDA reports)
BRAIN SCAN ABNORMAL ( 12 FDA reports)
CALCULUS URETERIC ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 12 FDA reports)
CAROTID BRUIT ( 12 FDA reports)
CERUMEN IMPACTION ( 12 FDA reports)
CHRONIC HEPATITIS ( 12 FDA reports)
COLECTOMY ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CONTRAST MEDIA REACTION ( 12 FDA reports)
CORONARY ARTERY OCCLUSION ( 12 FDA reports)
DENTAL NECROSIS ( 12 FDA reports)
DIET REFUSAL ( 12 FDA reports)
ENDOTRACHEAL INTUBATION ( 12 FDA reports)
ERUCTATION ( 12 FDA reports)
FAECALOMA ( 12 FDA reports)
FEELING COLD ( 12 FDA reports)
FIBULA FRACTURE ( 12 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 12 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 12 FDA reports)
GUILLAIN-BARRE SYNDROME ( 12 FDA reports)
HEMIPARESIS ( 12 FDA reports)
HISTAMINE LEVEL INCREASED ( 12 FDA reports)
INFUSION RELATED REACTION ( 12 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 12 FDA reports)
KNEE ARTHROPLASTY ( 12 FDA reports)
KYPHOSCOLIOSIS ( 12 FDA reports)
LEUKOCYTURIA ( 12 FDA reports)
LICHEN PLANUS ( 12 FDA reports)
LICHENOID KERATOSIS ( 12 FDA reports)
LOWER LIMB FRACTURE ( 12 FDA reports)
MENSTRUATION IRREGULAR ( 12 FDA reports)
METRORRHAGIA ( 12 FDA reports)
MUSCLE TIGHTNESS ( 12 FDA reports)
NEUROENDOCRINE CARCINOMA ( 12 FDA reports)
NON-CARDIAC CHEST PAIN ( 12 FDA reports)
OPTIC NERVE CUPPING ( 12 FDA reports)
ORAL DISCHARGE ( 12 FDA reports)
ORAL INFECTION ( 12 FDA reports)
PARAPARESIS ( 12 FDA reports)
PERICARDIAL CYST ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
POLYPECTOMY ( 12 FDA reports)
POST PROCEDURAL INFECTION ( 12 FDA reports)
POSTOPERATIVE INFECTION ( 12 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 12 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 12 FDA reports)
PYELOCALIECTASIS ( 12 FDA reports)
REFLUX GASTRITIS ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
RETCHING ( 12 FDA reports)
RIGHT ATRIAL DILATATION ( 12 FDA reports)
SKIN INDURATION ( 12 FDA reports)
SKIN PLAQUE ( 12 FDA reports)
STATUS EPILEPTICUS ( 12 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 12 FDA reports)
THERAPY NON-RESPONDER ( 12 FDA reports)
THIRST ( 12 FDA reports)
THROMBOPHLEBITIS ( 12 FDA reports)
URETHRAL CARUNCLE ( 12 FDA reports)
VAGINAL DISCHARGE ( 12 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 11 FDA reports)
ADNEXA UTERI MASS ( 11 FDA reports)
ANAL ABSCESS ( 11 FDA reports)
ANGIOPATHY ( 11 FDA reports)
APPENDICITIS PERFORATED ( 11 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 11 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 11 FDA reports)
ASTROCYTOMA ( 11 FDA reports)
AXILLARY PAIN ( 11 FDA reports)
BASEDOW'S DISEASE ( 11 FDA reports)
BIFASCICULAR BLOCK ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BLADDER DISORDER ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
BONE FISTULA ( 11 FDA reports)
BREAST CANCER ( 11 FDA reports)
BREAST DISCHARGE ( 11 FDA reports)
BREAST MASS ( 11 FDA reports)
CATARACT NUCLEAR ( 11 FDA reports)
CERVICITIS ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 11 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 11 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 11 FDA reports)
DELUSION ( 11 FDA reports)
DIAPHRAGMATIC HERNIA ( 11 FDA reports)
DISORDER OF ORBIT ( 11 FDA reports)
DRUG DISPENSING ERROR ( 11 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 11 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 11 FDA reports)
ENDOMETRIAL CANCER ( 11 FDA reports)
EXANTHEM ( 11 FDA reports)
GENITAL CANDIDIASIS ( 11 FDA reports)
HERNIA ( 11 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 11 FDA reports)
INCREASED BRONCHIAL SECRETION ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
LAGOPHTHALMOS ( 11 FDA reports)
LIP DRY ( 11 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 11 FDA reports)
MALLORY-WEISS SYNDROME ( 11 FDA reports)
MASTOCYTOSIS ( 11 FDA reports)
MEDIASTINAL DISORDER ( 11 FDA reports)
METABOLIC ENCEPHALOPATHY ( 11 FDA reports)
METASTASES TO HEART ( 11 FDA reports)
METASTASES TO THE MEDIASTINUM ( 11 FDA reports)
MITRAL VALVE SCLEROSIS ( 11 FDA reports)
MULTI-ORGAN DISORDER ( 11 FDA reports)
MUSCLE ATROPHY ( 11 FDA reports)
MYOFASCITIS ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NECROSIS ( 11 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 11 FDA reports)
OMENTUM NEOPLASM ( 11 FDA reports)
OROPHARYNGEAL BLISTERING ( 11 FDA reports)
PALMAR ERYTHEMA ( 11 FDA reports)
PANCREATIC CARCINOMA ( 11 FDA reports)
PARAPROTEINAEMIA ( 11 FDA reports)
PARONYCHIA ( 11 FDA reports)
PARTIAL SEIZURES ( 11 FDA reports)
PERIRECTAL ABSCESS ( 11 FDA reports)
PERNICIOUS ANAEMIA ( 11 FDA reports)
PHOTOPSIA ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 11 FDA reports)
PREGNANCY ( 11 FDA reports)
RADICULITIS CERVICAL ( 11 FDA reports)
RENAL OSTEODYSTROPHY ( 11 FDA reports)
RENAL TUBULAR DISORDER ( 11 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 11 FDA reports)
RETICULOCYTE COUNT INCREASED ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
RHONCHI ( 11 FDA reports)
RIB DEFORMITY ( 11 FDA reports)
SEBORRHOEIC DERMATITIS ( 11 FDA reports)
SECONDARY SEQUESTRUM ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SERRATIA INFECTION ( 11 FDA reports)
SKIN SWELLING ( 11 FDA reports)
SMALL INTESTINE OPERATION ( 11 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 11 FDA reports)
SPINAL OPERATION ( 11 FDA reports)
SPLENIC CYST ( 11 FDA reports)
STOMACH DISCOMFORT ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TONGUE DISORDER ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
VITAMIN D DEFICIENCY ( 11 FDA reports)
VULVOVAGINAL DRYNESS ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 10 FDA reports)
AGEUSIA ( 10 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 10 FDA reports)
ALVEOLITIS ALLERGIC ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 10 FDA reports)
AUTOIMMUNE DISORDER ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BALANOPOSTHITIS ( 10 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
BLADDER CANCER ( 10 FDA reports)
BLOOD OSMOLARITY DECREASED ( 10 FDA reports)
BONE CYST ( 10 FDA reports)
BONE MARROW DISORDER ( 10 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 10 FDA reports)
BONE SWELLING ( 10 FDA reports)
BREAST HAEMATOMA ( 10 FDA reports)
BRONCHOPNEUMOPATHY ( 10 FDA reports)
BUNION OPERATION ( 10 FDA reports)
CARDIAC OPERATION ( 10 FDA reports)
CATHETER SITE HAEMORRHAGE ( 10 FDA reports)
CELL DEATH ( 10 FDA reports)
COLONOSCOPY ( 10 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 10 FDA reports)
COORDINATION ABNORMAL ( 10 FDA reports)
COR PULMONALE ( 10 FDA reports)
CORONARY ARTERY BYPASS ( 10 FDA reports)
COW'S MILK INTOLERANCE ( 10 FDA reports)
DEFAECATION URGENCY ( 10 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 10 FDA reports)
DERMOID CYST ( 10 FDA reports)
DIABETIC COMA ( 10 FDA reports)
DRUG ABUSER ( 10 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 10 FDA reports)
EMBOLISM ARTERIAL ( 10 FDA reports)
ENDOSCOPY ( 10 FDA reports)
EPIDIDYMAL CYST ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
FACIAL BONES FRACTURE ( 10 FDA reports)
FOLLICULITIS ( 10 FDA reports)
GAMMOPATHY ( 10 FDA reports)
GLOBULINS INCREASED ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
HALLUCINATION, AUDITORY ( 10 FDA reports)
HAND FRACTURE ( 10 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 10 FDA reports)
HYPERVENTILATION ( 10 FDA reports)
HYPOPROTEINAEMIA ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
LEUKODYSTROPHY ( 10 FDA reports)
LIGAMENT RUPTURE ( 10 FDA reports)
LIMB DISCOMFORT ( 10 FDA reports)
LORDOSIS ( 10 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 10 FDA reports)
LYMPHADENITIS ( 10 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
MILIA ( 10 FDA reports)
MITRAL VALVE DISEASE ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
OESOPHAGEAL POLYP ( 10 FDA reports)
OPEN FRACTURE ( 10 FDA reports)
ORAL INTAKE REDUCED ( 10 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 10 FDA reports)
OSTEOMYELITIS ACUTE ( 10 FDA reports)
PANCREATIC ATROPHY ( 10 FDA reports)
PANCREATIC CYST ( 10 FDA reports)
PANIC REACTION ( 10 FDA reports)
PERICARDIAL DISEASE ( 10 FDA reports)
PERIODONTAL INFECTION ( 10 FDA reports)
PERIORBITAL OEDEMA ( 10 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 10 FDA reports)
PULMONARY EOSINOPHILIA ( 10 FDA reports)
REFLUX LARYNGITIS ( 10 FDA reports)
RESPIRATORY RATE INCREASED ( 10 FDA reports)
SCROTAL ABSCESS ( 10 FDA reports)
SCROTAL INFECTION ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SHOULDER ARTHROPLASTY ( 10 FDA reports)
SKIN NEOPLASM EXCISION ( 10 FDA reports)
SKIN WARM ( 10 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 10 FDA reports)
SPLENIC INFARCTION ( 10 FDA reports)
SUBDURAL HAEMORRHAGE ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TENDON INJURY ( 10 FDA reports)
THINKING ABNORMAL ( 10 FDA reports)
THROMBOSIS IN DEVICE ( 10 FDA reports)
THYROID ADENOMA ( 10 FDA reports)
THYROID MASS ( 10 FDA reports)
TONGUE ULCERATION ( 10 FDA reports)
URETHRAL STENOSIS ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VAGINAL INFECTION ( 10 FDA reports)
VAGINITIS BACTERIAL ( 10 FDA reports)
VARICELLA ( 10 FDA reports)
ACUTE STRESS DISORDER ( 9 FDA reports)
ADDISON'S DISEASE ( 9 FDA reports)
ANAL INFLAMMATION ( 9 FDA reports)
ANEURYSM ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 9 FDA reports)
AORTIC VALVE STENOSIS ( 9 FDA reports)
APATHY ( 9 FDA reports)
BACTERIAL SEPSIS ( 9 FDA reports)
BLINDNESS TRANSIENT ( 9 FDA reports)
BLOOD CHLORIDE DECREASED ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 9 FDA reports)
BRAIN OPERATION ( 9 FDA reports)
BREAST LUMP REMOVAL ( 9 FDA reports)
BUTTOCK PAIN ( 9 FDA reports)
COAGULATION FACTOR DECREASED ( 9 FDA reports)
CYSTOCELE ( 9 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 9 FDA reports)
DIABETIC FOOT ( 9 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 9 FDA reports)
DYSLEXIA ( 9 FDA reports)
EJECTION FRACTION ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 9 FDA reports)
ENANTHEMA ( 9 FDA reports)
ENCEPHALITIS HERPES ( 9 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 9 FDA reports)
ENDOMETRIAL ATROPHY ( 9 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 9 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 9 FDA reports)
EPICONDYLITIS ( 9 FDA reports)
EPIDERMAL NECROSIS ( 9 FDA reports)
ESCHAR ( 9 FDA reports)
EXTRASYSTOLES ( 9 FDA reports)
FANCONI SYNDROME ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
FUNGAL SKIN INFECTION ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 9 FDA reports)
GRANULOCYTES MATURATION ARREST ( 9 FDA reports)
HAEMORRHAGIC DISORDER ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEPATORENAL SYNDROME ( 9 FDA reports)
HIP DEFORMITY ( 9 FDA reports)
HOSPITALISATION ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
HYPERREFLEXIA ( 9 FDA reports)
HYPERSOMNIA ( 9 FDA reports)
HYPERURICAEMIA ( 9 FDA reports)
HYSTERECTOMY ( 9 FDA reports)
INCISION SITE INFECTION ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 9 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 9 FDA reports)
ISCHAEMIC STROKE ( 9 FDA reports)
JOINT CREPITATION ( 9 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 9 FDA reports)
LIP EROSION ( 9 FDA reports)
LIP PAIN ( 9 FDA reports)
LISTLESS ( 9 FDA reports)
LUNG CANCER METASTATIC ( 9 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 9 FDA reports)
LYMPHANGITIS ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MEDIASTINUM NEOPLASM ( 9 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 9 FDA reports)
MONOPLEGIA ( 9 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 9 FDA reports)
NERVE COMPRESSION ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 9 FDA reports)
OSTEOCHONDROSIS ( 9 FDA reports)
PARANASAL SINUS DISCOMFORT ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PERICARDITIS ( 9 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 9 FDA reports)
PITTING OEDEMA ( 9 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 9 FDA reports)
PROSTATITIS ( 9 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 9 FDA reports)
RETINAL VASCULAR DISORDER ( 9 FDA reports)
RHINITIS SEASONAL ( 9 FDA reports)
SEBACEOUS GLAND DISORDER ( 9 FDA reports)
SKIN TEST NEGATIVE ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SPEECH REHABILITATION ( 9 FDA reports)
SPONDYLITIS ( 9 FDA reports)
STREPTOCOCCAL SEPSIS ( 9 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 9 FDA reports)
SUFFOCATION FEELING ( 9 FDA reports)
SYNOVITIS ( 9 FDA reports)
THYROID CYST ( 9 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 9 FDA reports)
TOXIC NODULAR GOITRE ( 9 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 9 FDA reports)
TRAUMATIC HAEMATOMA ( 9 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 9 FDA reports)
UMBILICAL HERNIA ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 9 FDA reports)
VERTIGO POSITIONAL ( 9 FDA reports)
WOUND DEHISCENCE ( 9 FDA reports)
WOUND TREATMENT ( 9 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ADHESION ( 8 FDA reports)
ANAL FISTULA ( 8 FDA reports)
ANGIOLIPOMA ( 8 FDA reports)
APLASIA ( 8 FDA reports)
AREFLEXIA ( 8 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 8 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 8 FDA reports)
ARTERITIS ( 8 FDA reports)
ASBESTOSIS ( 8 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 8 FDA reports)
BILIARY CIRRHOSIS ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD CREATINE INCREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
BODY DYSMORPHIC DISORDER ( 8 FDA reports)
BONE SARCOMA ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BRONCHIAL OBSTRUCTION ( 8 FDA reports)
CARDIAC ANEURYSM ( 8 FDA reports)
CARDIAC TAMPONADE ( 8 FDA reports)
CARDIOPULMONARY FAILURE ( 8 FDA reports)
CHANGE OF BOWEL HABIT ( 8 FDA reports)
CHARLES BONNET SYNDROME ( 8 FDA reports)
CHOLURIA ( 8 FDA reports)
CHRONIC TONSILLITIS ( 8 FDA reports)
CLAVICLE FRACTURE ( 8 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 8 FDA reports)
COLLAPSE OF LUNG ( 8 FDA reports)
COLON NEOPLASM ( 8 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 8 FDA reports)
CONGENITAL ANOMALY ( 8 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 8 FDA reports)
CONGENITAL TRACHEOMALACIA ( 8 FDA reports)
CONJUNCTIVAL DISORDER ( 8 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 8 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 8 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 8 FDA reports)
CUSHINGOID ( 8 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 8 FDA reports)
DENTOFACIAL ANOMALY ( 8 FDA reports)
DEXTROCARDIA ( 8 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 8 FDA reports)
DYSPNOEA EXACERBATED ( 8 FDA reports)
EAR NEOPLASM ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 8 FDA reports)
ENCEPHALITIS ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
ENTEROVESICAL FISTULA ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
EYE OEDEMA ( 8 FDA reports)
EYELID PTOSIS ( 8 FDA reports)
FACIAL PALSY ( 8 FDA reports)
FAMILY STRESS ( 8 FDA reports)
FIBROMA ( 8 FDA reports)
FOREIGN BODY ( 8 FDA reports)
GASTRITIS ATROPHIC ( 8 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 8 FDA reports)
GRIMACING ( 8 FDA reports)
HAIR GROWTH ABNORMAL ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HEART SOUNDS ABNORMAL ( 8 FDA reports)
HEPATIC HAEMATOMA ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HYPERPHAGIA ( 8 FDA reports)
IMPAIRED DRIVING ABILITY ( 8 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 8 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
INTRACRANIAL ANEURYSM ( 8 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 8 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 8 FDA reports)
ISCHAEMIC HEPATITIS ( 8 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 8 FDA reports)
LYMPHOCYTIC INFILTRATION ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
NASAL MUCOSAL DISORDER ( 8 FDA reports)
NEUROSIS ( 8 FDA reports)
NIGHT BLINDNESS ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 8 FDA reports)
OBSTRUCTION GASTRIC ( 8 FDA reports)
OPTIC NERVE INJURY ( 8 FDA reports)
ORAL MUCOSA EROSION ( 8 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PNEUMONIA MYCOPLASMAL ( 8 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
POST HERPETIC NEURALGIA ( 8 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 8 FDA reports)
PROCEDURAL COMPLICATION ( 8 FDA reports)
PULMONARY VASCULAR DISORDER ( 8 FDA reports)
PUSTULAR PSORIASIS ( 8 FDA reports)
PYURIA ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RENAL INFARCT ( 8 FDA reports)
SCRATCH ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SKIN CYST EXCISION ( 8 FDA reports)
SKIN DESQUAMATION ( 8 FDA reports)
SKIN INFLAMMATION ( 8 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
SYNOVIAL RUPTURE ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
TERMINAL STATE ( 8 FDA reports)
TONGUE BLACK HAIRY ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
TOOTH DEPOSIT ( 8 FDA reports)
TUMOUR NECROSIS ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
URINE ABNORMALITY ( 8 FDA reports)
UTERINE PROLAPSE ( 8 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 7 FDA reports)
ACCIDENT AT WORK ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
AMINOACIDURIA ( 7 FDA reports)
ANAPHYLACTOID SHOCK ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
APICECTOMY ( 7 FDA reports)
ARTERIOVENOUS FISTULA ( 7 FDA reports)
BALANITIS CANDIDA ( 7 FDA reports)
BENIGN OVARIAN TUMOUR ( 7 FDA reports)
BILIARY COLIC ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BIOPSY GINGIVAL ( 7 FDA reports)
BIPOLAR I DISORDER ( 7 FDA reports)
BLEEDING TIME PROLONGED ( 7 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BONE MARROW OEDEMA ( 7 FDA reports)
CALCULUS BLADDER ( 7 FDA reports)
CAPILLARY LEAK SYNDROME ( 7 FDA reports)
CEREBRAL PALSY ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 7 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 7 FDA reports)
COAGULATION TIME PROLONGED ( 7 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 7 FDA reports)
COMMINUTED FRACTURE ( 7 FDA reports)
CONJUNCTIVAL OEDEMA ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
CYSTITIS INTERSTITIAL ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DERMATOSIS ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DUODENAL POLYP ( 7 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 7 FDA reports)
DYSTHYMIC DISORDER ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
ENTEROCELE ( 7 FDA reports)
EXTRASKELETAL OSSIFICATION ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
FACET JOINT BLOCK ( 7 FDA reports)
FAT NECROSIS ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 7 FDA reports)
FLUID INTAKE REDUCED ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
GASTRIC CANCER RECURRENT ( 7 FDA reports)
GENITAL EROSION ( 7 FDA reports)
GINGIVAL OEDEMA ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HELICOBACTER INFECTION ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HERPES VIRUS INFECTION ( 7 FDA reports)
HYPERAMMONAEMIA ( 7 FDA reports)
HYPOCAPNIA ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
JOINT CONTRACTURE ( 7 FDA reports)
LACUNAR INFARCTION ( 7 FDA reports)
LIGAMENT INJURY ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LUNG INJURY ( 7 FDA reports)
LYMPH NODE PALPABLE ( 7 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 7 FDA reports)
MANDIBULAR PROSTHESIS USER ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
MENOPAUSAL SYMPTOMS ( 7 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 7 FDA reports)
METASTASES TO ABDOMINAL WALL ( 7 FDA reports)
METASTASES TO PANCREAS ( 7 FDA reports)
METASTATIC PAIN ( 7 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 7 FDA reports)
MOUTH CYST ( 7 FDA reports)
MYOCARDITIS ( 7 FDA reports)
NASAL OEDEMA ( 7 FDA reports)
NEUROGENIC BLADDER ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER ( 7 FDA reports)
ORTHOPEDIC PROCEDURE ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
PANCREATIC ENLARGEMENT ( 7 FDA reports)
PANCREATIC MASS ( 7 FDA reports)
PERIPHERAL NERVE INJURY ( 7 FDA reports)
PLEURITIC PAIN ( 7 FDA reports)
POOR PERIPHERAL CIRCULATION ( 7 FDA reports)
PROSTATE INFECTION ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 7 FDA reports)
PULSE PRESSURE DECREASED ( 7 FDA reports)
RADICULAR CYST ( 7 FDA reports)
RECTOCELE ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RENAL ARTERY STENOSIS ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RETICULOCYTOSIS ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SCROTAL CYST ( 7 FDA reports)
SELF-MEDICATION ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SKIN ODOUR ABNORMAL ( 7 FDA reports)
SKIN TIGHTNESS ( 7 FDA reports)
SMEAR CERVIX ABNORMAL ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
SPLENIC CALCIFICATION ( 7 FDA reports)
SPUTUM PURULENT ( 7 FDA reports)
STILLBIRTH ( 7 FDA reports)
STRESS URINARY INCONTINENCE ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TENDINOUS CONTRACTURE ( 7 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 7 FDA reports)
TOE AMPUTATION ( 7 FDA reports)
TRACHEOSTOMY ( 7 FDA reports)
TYPE I HYPERSENSITIVITY ( 7 FDA reports)
URINE COLOUR ABNORMAL ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VESTIBULAR DISORDER ( 7 FDA reports)
VIRAL PHARYNGITIS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VULVAR DYSPLASIA ( 6 FDA reports)
VULVITIS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ABSCESS MANAGEMENT ( 6 FDA reports)
ACHOLIA ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
ANORECTAL DISORDER ( 6 FDA reports)
ANTIBODY TEST POSITIVE ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
BREAST CANCER RECURRENT ( 6 FDA reports)
BRONCHIOLITIS ( 6 FDA reports)
CARDIAC FAILURE ACUTE ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHOKING SENSATION ( 6 FDA reports)
CLAUSTROPHOBIA ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
EAR IRRIGATION ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
EYELID FUNCTION DISORDER ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FULL BLOOD COUNT DECREASED ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GALLBLADDER INJURY ( 6 FDA reports)
GASTRECTOMY ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GENITOURINARY TRACT INFECTION ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HEPATIC INFARCTION ( 6 FDA reports)
HERNIA REPAIR ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HISTOPLASMOSIS ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERPHOSPHATAEMIA ( 6 FDA reports)
HYPOGLYCAEMIC COMA ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
LACRIMAL DISORDER ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LIVEDO RETICULARIS ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
LUNG HYPERINFLATION ( 6 FDA reports)
MAGNESIUM DEFICIENCY ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 6 FDA reports)
MAXILLOFACIAL OPERATION ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTASES TO MENINGES ( 6 FDA reports)
METASTASES TO SPLEEN ( 6 FDA reports)
MITRAL VALVE REPLACEMENT ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
MUCOSAL HAEMORRHAGE ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MURPHY'S SIGN POSITIVE ( 6 FDA reports)
MYELOFIBROSIS ( 6 FDA reports)
MYELOID LEUKAEMIA ( 6 FDA reports)
MYOPERICARDITIS ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 6 FDA reports)
NEUTROPENIC INFECTION ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OEDEMA GENITAL ( 6 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OESOPHAGEAL SPASM ( 6 FDA reports)
OPEN WOUND ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 6 FDA reports)
PARANOIA ( 6 FDA reports)
PARKINSONISM ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PERSONALITY DISORDER ( 6 FDA reports)
POLYHYDRAMNIOS ( 6 FDA reports)
POST PROCEDURAL DISCHARGE ( 6 FDA reports)
POST PROCEDURAL HAEMATURIA ( 6 FDA reports)
PREMATURE LABOUR ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PROSTATECTOMY ( 6 FDA reports)
PROSTATIC OBSTRUCTION ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RED MAN SYNDROME ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SINUS ANTROSTOMY ( 6 FDA reports)
SOFT TISSUE MASS ( 6 FDA reports)
SOPOR ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
SPLINT APPLICATION ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SUPERINFECTION LUNG ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TESTICULAR ATROPHY ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
TOOTH DISCOLOURATION ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 6 FDA reports)
TRANSFUSION REACTION ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRIGEMINAL NEURALGIA ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 6 FDA reports)
UVEITIS ( 6 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 5 FDA reports)
ADENOIDAL HYPERTROPHY ( 5 FDA reports)
ADENOTONSILLECTOMY ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ALLERGIC BRONCHITIS ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANAL FISSURE ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
ANIMAL SCRATCH ( 5 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 5 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 5 FDA reports)
APHONIA ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 5 FDA reports)
ASPLENIA ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
BREAST CALCIFICATIONS ( 5 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 5 FDA reports)
BULIMIA NERVOSA ( 5 FDA reports)
BULLOUS LUNG DISEASE ( 5 FDA reports)
CALCIPHYLAXIS ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CERUMEN REMOVAL ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHOKING ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHOLESTEROSIS ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
COAGULATION TEST ABNORMAL ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
CONDUCTION DISORDER ( 5 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 5 FDA reports)
CRANIOSYNOSTOSIS ( 5 FDA reports)
CROUP INFECTIOUS ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
CUTIS LAXA ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DENTAL IMPLANTATION ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DERMATITIS ATOPIC ( 5 FDA reports)
DERMOGRAPHISM ( 5 FDA reports)
DIABETIC COMPLICATION ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DIPLEGIA ( 5 FDA reports)
DIZZINESS POSTURAL ( 5 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 5 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROPHORESIS ABNORMAL ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
FEEDING DISORDER NEONATAL ( 5 FDA reports)
FEELING GUILTY ( 5 FDA reports)
FIBROUS HISTIOCYTOMA ( 5 FDA reports)
FOETAL DISTRESS SYNDROME ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GENITAL ULCERATION ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMORRHAGIC ANAEMIA ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC TRAUMA ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 5 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 5 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
HYPOPROTHROMBINAEMIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
KNEE OPERATION ( 5 FDA reports)
LARYNGEAL STENOSIS ( 5 FDA reports)
LARYNGOSCOPY ( 5 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MARROW HYPERPLASIA ( 5 FDA reports)
MASTOIDITIS ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MEIBOMIANITIS ( 5 FDA reports)
MENINGEAL NEOPLASM ( 5 FDA reports)
MENINGITIS ASEPTIC ( 5 FDA reports)
MENINGOCELE ( 5 FDA reports)
MENTAL IMPAIRMENT ( 5 FDA reports)
MERALGIA PARAESTHETICA ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
NARCOTIC INTOXICATION ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OEDEMATOUS PANCREATITIS ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
OPEN ANGLE GLAUCOMA ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
PAPILLOMA ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PIGMENTATION DISORDER ( 5 FDA reports)
PINGUECULA ( 5 FDA reports)
PLASMA CELLS INCREASED ( 5 FDA reports)
PLEURECTOMY ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
POLYCYSTIC OVARIES ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
POLYTRAUMATISM ( 5 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PSEUDOMONAL SEPSIS ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PSYCHOTHERAPY ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RECTAL TENESMUS ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETINOL BINDING PROTEIN INCREASED ( 5 FDA reports)
RHABDOMYOMA ( 5 FDA reports)
RHABDOMYOSARCOMA ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SHOULDER OPERATION ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SITUS INVERSUS ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SPINAL DECOMPRESSION ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
SYMBLEPHARON ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THORACOTOMY ( 5 FDA reports)
THROMBECTOMY ( 5 FDA reports)
THYROIDECTOMY ( 5 FDA reports)
TINEA CRURIS ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TOE DEFORMITY ( 5 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
TOOTH HYPOPLASIA ( 5 FDA reports)
TORTICOLLIS ( 5 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 5 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 5 FDA reports)
TREATMENT FAILURE ( 5 FDA reports)
TROPONIN T INCREASED ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
TUBEROUS SCLEROSIS ( 5 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
ULNAR NERVE INJURY ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URETERAL NEOPLASM ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
UTERINE MALPOSITION ( 5 FDA reports)
VAGOTOMY ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
VIBRATION TEST ABNORMAL ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 5 FDA reports)
WRIST FRACTURE ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
VASCULAR ENCEPHALOPATHY ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VULVOVAGINITIS ( 4 FDA reports)
WHIPLASH INJURY ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
ALPHA 1 MICROGLOBULIN INCREASED ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
AMYOTROPHY ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANION GAP INCREASED ( 4 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 4 FDA reports)
ANTI FACTOR V ANTIBODY POSITIVE ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
ASPIRATION JOINT ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 4 FDA reports)
BICYTOPENIA ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BILIARY CYST ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BRADYCARDIA NEONATAL ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
BRONCHOMALACIA ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
CAMPYLOBACTER INFECTION ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CELLULITIS GANGRENOUS ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 4 FDA reports)
CHOLANGITIS SCLEROSING ( 4 FDA reports)
CHOLESTEATOMA ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
CLUBBING ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COLONIC STENOSIS ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CRYSTAL URINE ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
CUTANEOUS VASCULITIS ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 4 FDA reports)
DENTAL CARE ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DUODENAL FISTULA ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSHIDROSIS ( 4 FDA reports)
DYSMENORRHOEA ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
ESCHERICHIA TEST POSITIVE ( 4 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXOMPHALOS ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOOT OPERATION ( 4 FDA reports)
FORCEPS DELIVERY ( 4 FDA reports)
FUMBLING ( 4 FDA reports)
GALLBLADDER OEDEMA ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTROENTERITIS HELICOBACTER ( 4 FDA reports)
GASTROENTERITIS RADIATION ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GENITAL ERYTHEMA ( 4 FDA reports)
GENITAL INFECTION FUNGAL ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
GRAM STAIN POSITIVE ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HEPATIC VEIN THROMBOSIS ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HIGH FREQUENCY ABLATION ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYDROURETER ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE THROMBOSIS ( 4 FDA reports)
INJECTION SITE URTICARIA ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
IRITIS ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 4 FDA reports)
JAW LESION EXCISION ( 4 FDA reports)
JOINT SURGERY ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LARYNGEAL DISORDER ( 4 FDA reports)
LINEAR IGA DISEASE ( 4 FDA reports)
LOCAL REACTION ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LUNG CREPITATION ( 4 FDA reports)
LYMPHANGIECTASIA ( 4 FDA reports)
LYMPHATIC DISORDER ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MALARIA ( 4 FDA reports)
MALIGNANT TUMOUR EXCISION ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
METATARSUS PRIMUS VARUS ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MITRAL VALVE REPAIR ( 4 FDA reports)
MONOCYTOPENIA ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NERVE ROOT INJURY LUMBAR ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
OXYGEN SATURATION ABNORMAL ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PANCREATIC DUCT DILATATION ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PENILE INFECTION ( 4 FDA reports)
PERINEAL ABSCESS ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PERSISTENT LEFT SUPERIOR VENA CAVA ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PIGMENTARY GLAUCOMA ( 4 FDA reports)
PLAGIOCEPHALY ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PREMATURE DELIVERY ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PULMONARY NECROSIS ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RECTOCELE REPAIR ( 4 FDA reports)
RENAL ARTERY OCCLUSION ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESPIRATORY RATE ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN OPERATION ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
SPINAL CLAUDICATION ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SWOLLEN TEAR DUCT ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
TENSION ( 4 FDA reports)
TETANUS ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TRACHEAL INJURY ( 4 FDA reports)
TRACHEITIS ( 4 FDA reports)
TRANSPLANT ABSCESS ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URETHRAL STENT INSERTION ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABNORMAL CLOTTING FACTOR ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACCIDENTAL DEATH ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ADENOIDECTOMY ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALVEOLAR OSTEITIS ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAEMIA NEONATAL ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATELECTASIS NEONATAL ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
AZOOSPERMIA ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BICUSPID AORTIC VALVE ( 3 FDA reports)
BILIARY SEPSIS ( 3 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
BREAST NEOPLASM ( 3 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRONCHIAL HYPERACTIVITY ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
CALCIFICATION METASTATIC ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARDIAC AMYLOIDOSIS ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CHOLANGIOLITIS ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CIRCUMORAL OEDEMA ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 3 FDA reports)
COARCTATION OF THE AORTA ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 3 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 3 FDA reports)
CONJUNCTIVAL PALLOR ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CREATININE URINE INCREASED ( 3 FDA reports)
CROSS SENSITIVITY REACTION ( 3 FDA reports)
CRYSTALLURIA ( 3 FDA reports)
CULTURE STOOL NEGATIVE ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
DACRYOCYSTORHINOSTOMY ( 3 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIAPHRAGMATIC DISORDER ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 3 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
ENTEROBACTER BACTERAEMIA ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
ERYTHROSIS ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE NAEVUS ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FACTOR IX INHIBITION ( 3 FDA reports)
FAILURE TO ANASTOMOSE ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FOETAL CARDIAC DISORDER ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
FUNGAL TEST POSITIVE ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GLOMERULONEPHROPATHY ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERMETABOLISM ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOCOAGULABLE STATE ( 3 FDA reports)
HYPOPLASTIC ANAEMIA ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
IMPINGEMENT SYNDROME ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 3 FDA reports)
JUVENILE ARTHRITIS ( 3 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 3 FDA reports)
LACRIMAL DUCT PROCEDURE ( 3 FDA reports)
LACTOBACILLUS INFECTION ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LESION EXCISION ( 3 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LIVIDITY ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MANIA ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 3 FDA reports)
MEDICATION CRYSTALS IN URINE ( 3 FDA reports)
MEDICATION RESIDUE ( 3 FDA reports)
MENINGITIS TUBERCULOUS ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
METASTASES TO PLEURA ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYOFASCIAL SPASM ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NAIL HYPERTROPHY ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL FISTULA ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 3 FDA reports)
ONYCHALGIA ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PENILE OEDEMA ( 3 FDA reports)
PERIHEPATIC ABSCESS ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERITONITIS SCLEROSING ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHLEBOLITH ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PITYRIASIS ( 3 FDA reports)
PLEURAL HAEMORRHAGE ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONIA NECROTISING ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE THROMBOSIS ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
PRE-EXISTING DISEASE ( 3 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROPOFOL INFUSION SYNDROME ( 3 FDA reports)
PRURITUS ALLERGIC ( 3 FDA reports)
PRURITUS ANI ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETROSTERNAL INFECTION ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN LESION EXCISION ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SODIUM RETENTION ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC GRANULOMA ( 3 FDA reports)
SPONDYLOSIS ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STASIS DERMATITIS ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 3 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
URETERAL STENT INSERTION ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
UTERINE FIBROSIS ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINAL CELLULITIS ( 3 FDA reports)
VAGINAL ULCERATION ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VENIPUNCTURE SITE INFLAMMATION ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VESICOURETERIC REFLUX ( 3 FDA reports)
VIRAL TONSILLITIS ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VENOUS LAKE ( 2 FDA reports)
VENTRICLE RUPTURE ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE ENDOCARDITIS ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMAUROSIS FUGAX ( 2 FDA reports)
ANAEMIA OF PREGNANCY ( 2 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL BRUIT ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATROPHIC GLOSSITIS ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BARBITURATES POSITIVE ( 2 FDA reports)
BARTHOLIN'S ABSCESS ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY FISTULA ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD STEM CELL HARVEST ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH SOUNDS ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETERISATION VENOUS ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CERULOPLASMIN INCREASED ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 2 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COMA NEONATAL ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL PNEUMONIA ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CREATINE URINE INCREASED ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DERMATITIS DIAPER ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DYSPLASTIC NAEVUS ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR LOBE INFECTION ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
END-TIDAL CO2 DECREASED ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERB'S PALSY ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FAECAL VOLUME DECREASED ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GALLBLADDER NECROSIS ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GINGIVAL GRAFT ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRANULOCYTES ABNORMAL ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GROSS MOTOR DELAY ( 2 FDA reports)
HAEMATOMETRA ( 2 FDA reports)
HAEMOGLOBIN S DECREASED ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
ILIUM FRACTURE ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGEAL DYSPNOEA ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MACROPHAGE ACTIVATION ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METATARSAL EXCISION ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROSIS OF BRONCHIOLI ( 2 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 2 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 2 FDA reports)
NEISSERIA INFECTION ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
ODONTOGENIC CYST ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYDACTYLY ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PROSTATIC CALCIFICATION ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY ARTERY STENOSIS ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RADIOTHERAPY TO BRAIN ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRYPTASE ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACETONAEMIC VOMITING ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACRODERMATITIS ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
AMNIOTIC CAVITY DISORDER ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FUNGAL INFECTION ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLEPHAROSYNECHIA ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BONE MARROW EOSINOPHILIC LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID PULSE ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 1 FDA reports)
CHLAMYDIA TEST POSITIVE ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHONDROMA ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ACROCHORDON ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION FEMALE ( 1 FDA reports)
CONGENITAL HEARING DISORDER ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHOENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FONTANELLE DEPRESSED ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE, OBSTRUCTIVE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL INFECTION ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA CONGENITAL ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS NEONATAL ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE AGGLUTININS ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPLANT SITE EROSION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED INSECT BITE ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME ABNORMAL ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LABOUR PAIN ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARYNGEAL DISCOMFORT ( 1 FDA reports)
LARYNGEAL GRANULOMA ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL EXCORIATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL VESTIBULITIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULAR FASCIITIS ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCULAR VASCULITIS ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
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PERIANAL FUNGAL INFECTION ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMORPHIC ERUPTION OF PREGNANCY ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
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PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
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PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADIOALLERGOSORBENT TEST POSITIVE ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL ACANTHOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL ROULEAUX FORMATION PRESENT ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
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RENAL ANEURYSM ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
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RENAL GRAFT LOSS ( 1 FDA reports)
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RENAL HYPOPLASIA ( 1 FDA reports)
RENAL LIPOMATOSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
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RETINAL DISORDER ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
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RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND HYPERTROPHY ( 1 FDA reports)
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SCAR PAIN ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
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SCROTAL ERYTHEMA ( 1 FDA reports)
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SECONDARY SYPHILIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
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SHIFT TO THE LEFT ( 1 FDA reports)
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SINUS POLYP ( 1 FDA reports)
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SLEEP INERTIA ( 1 FDA reports)
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