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

PYREXIA ( 915 FDA reports)
CROHN'S DISEASE ( 683 FDA reports)
DRUG INEFFECTIVE ( 569 FDA reports)
DIARRHOEA ( 482 FDA reports)
NAUSEA ( 476 FDA reports)
SEPSIS ( 424 FDA reports)
VOMITING ( 418 FDA reports)
DYSPNOEA ( 415 FDA reports)
PNEUMONIA ( 402 FDA reports)
DRUG INTERACTION ( 380 FDA reports)
WEIGHT DECREASED ( 367 FDA reports)
ANAEMIA ( 366 FDA reports)
ABDOMINAL PAIN ( 361 FDA reports)
PANCYTOPENIA ( 356 FDA reports)
FATIGUE ( 352 FDA reports)
LEUKOPENIA ( 347 FDA reports)
ARTHRALGIA ( 345 FDA reports)
HEADACHE ( 342 FDA reports)
ASTHENIA ( 327 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 322 FDA reports)
BLOOD CREATININE INCREASED ( 281 FDA reports)
MALAISE ( 266 FDA reports)
CONDITION AGGRAVATED ( 263 FDA reports)
PAIN ( 255 FDA reports)
THROMBOCYTOPENIA ( 255 FDA reports)
RENAL FAILURE ( 237 FDA reports)
RENAL FAILURE ACUTE ( 232 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 229 FDA reports)
HAEMOGLOBIN DECREASED ( 229 FDA reports)
RASH ( 227 FDA reports)
BASAL CELL CARCINOMA ( 223 FDA reports)
RESPIRATORY FAILURE ( 221 FDA reports)
RENAL IMPAIRMENT ( 220 FDA reports)
COUGH ( 219 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 211 FDA reports)
OEDEMA PERIPHERAL ( 210 FDA reports)
DIZZINESS ( 206 FDA reports)
URINARY TRACT INFECTION ( 201 FDA reports)
CHEST PAIN ( 194 FDA reports)
HYPERTENSION ( 186 FDA reports)
INFUSION RELATED REACTION ( 184 FDA reports)
MYALGIA ( 184 FDA reports)
COLITIS ULCERATIVE ( 179 FDA reports)
PAIN IN EXTREMITY ( 174 FDA reports)
HERPES ZOSTER ( 169 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 168 FDA reports)
DEATH ( 167 FDA reports)
INFECTION ( 167 FDA reports)
BACK PAIN ( 166 FDA reports)
MULTI-ORGAN FAILURE ( 162 FDA reports)
HYPOTENSION ( 161 FDA reports)
INJECTION SITE PAIN ( 154 FDA reports)
MUSCULAR WEAKNESS ( 153 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 151 FDA reports)
PLATELET COUNT DECREASED ( 151 FDA reports)
PLEURAL EFFUSION ( 147 FDA reports)
GAIT DISTURBANCE ( 143 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 141 FDA reports)
PRURITUS ( 138 FDA reports)
NEUTROPENIA ( 136 FDA reports)
FALL ( 134 FDA reports)
SEPTIC SHOCK ( 134 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 130 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 129 FDA reports)
TACHYCARDIA ( 129 FDA reports)
BONE MARROW FAILURE ( 128 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 126 FDA reports)
CHILLS ( 124 FDA reports)
SQUAMOUS CELL CARCINOMA ( 124 FDA reports)
LYMPHADENOPATHY ( 123 FDA reports)
ERYTHEMA ( 122 FDA reports)
DEPRESSION ( 120 FDA reports)
FISTULA ( 120 FDA reports)
INTESTINAL OBSTRUCTION ( 120 FDA reports)
PULMONARY EMBOLISM ( 120 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 120 FDA reports)
DEHYDRATION ( 119 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 119 FDA reports)
ABDOMINAL PAIN UPPER ( 118 FDA reports)
RHEUMATOID ARTHRITIS ( 118 FDA reports)
CONVULSION ( 116 FDA reports)
PROTEINURIA ( 116 FDA reports)
HYPERSENSITIVITY ( 114 FDA reports)
PARAESTHESIA ( 114 FDA reports)
BLOOD PRESSURE INCREASED ( 113 FDA reports)
HAEMODIALYSIS ( 113 FDA reports)
DEEP VEIN THROMBOSIS ( 111 FDA reports)
HYPOAESTHESIA ( 111 FDA reports)
NECK PAIN ( 111 FDA reports)
DECREASED APPETITE ( 110 FDA reports)
RHABDOMYOLYSIS ( 109 FDA reports)
ABORTION SPONTANEOUS ( 108 FDA reports)
DISEASE RECURRENCE ( 108 FDA reports)
ASCITES ( 107 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 107 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 105 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 105 FDA reports)
DIABETES MELLITUS ( 104 FDA reports)
INFLUENZA LIKE ILLNESS ( 104 FDA reports)
LYMPHOMA ( 104 FDA reports)
STAPHYLOCOCCAL INFECTION ( 104 FDA reports)
PREMATURE BABY ( 103 FDA reports)
ALOPECIA ( 102 FDA reports)
CAESAREAN SECTION ( 102 FDA reports)
CONFUSIONAL STATE ( 102 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 101 FDA reports)
TUBERCULOSIS ( 101 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 100 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 100 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 99 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 98 FDA reports)
CEREBROVASCULAR ACCIDENT ( 97 FDA reports)
JOINT SWELLING ( 97 FDA reports)
PREGNANCY ( 96 FDA reports)
TRANSPLANT REJECTION ( 95 FDA reports)
INCORRECT DOSE ADMINISTERED ( 94 FDA reports)
PANCREATITIS ( 93 FDA reports)
WEIGHT INCREASED ( 92 FDA reports)
BRONCHIECTASIS ( 91 FDA reports)
MYOCARDIAL INFARCTION ( 91 FDA reports)
ANXIETY ( 90 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 90 FDA reports)
RENAL FAILURE CHRONIC ( 90 FDA reports)
SKIN LESION ( 90 FDA reports)
APLASIA PURE RED CELL ( 87 FDA reports)
ASPERGILLOSIS ( 87 FDA reports)
HEPATITIS ( 86 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 85 FDA reports)
INTESTINAL PERFORATION ( 85 FDA reports)
TREMOR ( 85 FDA reports)
ATRIAL FIBRILLATION ( 84 FDA reports)
HOSPITALISATION ( 84 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 82 FDA reports)
DYSPHAGIA ( 82 FDA reports)
HEPATIC ENZYME INCREASED ( 82 FDA reports)
HEPATIC FAILURE ( 82 FDA reports)
INFLAMMATION ( 82 FDA reports)
INSOMNIA ( 82 FDA reports)
PULMONARY FIBROSIS ( 82 FDA reports)
ANOREXIA ( 81 FDA reports)
CARDIAC ARREST ( 81 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 81 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 80 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 79 FDA reports)
LUNG INFILTRATION ( 79 FDA reports)
CELLULITIS ( 78 FDA reports)
GASTROINTESTINAL DISORDER ( 78 FDA reports)
JAUNDICE ( 78 FDA reports)
LARGE INTESTINE PERFORATION ( 78 FDA reports)
PREMATURE LABOUR ( 78 FDA reports)
ABDOMINAL ABSCESS ( 77 FDA reports)
B-CELL LYMPHOMA ( 77 FDA reports)
RECTAL HAEMORRHAGE ( 77 FDA reports)
ABSCESS ( 76 FDA reports)
CHOLESTASIS ( 76 FDA reports)
HAEMATOCHEZIA ( 76 FDA reports)
COLITIS ( 75 FDA reports)
INJECTION SITE ERYTHEMA ( 75 FDA reports)
LOSS OF CONSCIOUSNESS ( 75 FDA reports)
MUSCLE SPASMS ( 75 FDA reports)
ABDOMINAL DISTENSION ( 74 FDA reports)
CONSTIPATION ( 74 FDA reports)
DRUG HYPERSENSITIVITY ( 74 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 73 FDA reports)
NEPHROPATHY TOXIC ( 73 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 73 FDA reports)
VASCULITIS ( 72 FDA reports)
BLOOD UREA INCREASED ( 72 FDA reports)
CARDIAC FAILURE ( 72 FDA reports)
DISEASE PROGRESSION ( 72 FDA reports)
SINUSITIS ( 72 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 71 FDA reports)
DISSEMINATED TUBERCULOSIS ( 71 FDA reports)
TRANSAMINASES INCREASED ( 71 FDA reports)
VISION BLURRED ( 71 FDA reports)
ACCIDENTAL EXPOSURE ( 69 FDA reports)
ANAL FISTULA ( 69 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 69 FDA reports)
MYELODYSPLASTIC SYNDROME ( 69 FDA reports)
ARTHRITIS ( 68 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 68 FDA reports)
CORONARY ARTERY DISEASE ( 68 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 68 FDA reports)
HYPERHIDROSIS ( 68 FDA reports)
OSTEOMYELITIS ( 68 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 67 FDA reports)
INTERSTITIAL LUNG DISEASE ( 67 FDA reports)
CHEST DISCOMFORT ( 66 FDA reports)
HYPOXIA ( 66 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 66 FDA reports)
POST PROCEDURAL COMPLICATION ( 66 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 65 FDA reports)
MALIGNANT MELANOMA ( 65 FDA reports)
VIRAL INFECTION ( 65 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 64 FDA reports)
ABDOMINAL DISCOMFORT ( 64 FDA reports)
IMMUNOSUPPRESSION ( 63 FDA reports)
PALPITATIONS ( 63 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 62 FDA reports)
HAEMATOCRIT DECREASED ( 62 FDA reports)
HEPATITIS CHOLESTATIC ( 62 FDA reports)
NASOPHARYNGITIS ( 62 FDA reports)
URTICARIA ( 62 FDA reports)
ANAL ABSCESS ( 61 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 61 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 60 FDA reports)
HAEMORRHAGE ( 60 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 60 FDA reports)
IMPAIRED HEALING ( 60 FDA reports)
RENAL DISORDER ( 60 FDA reports)
RESPIRATORY DISTRESS ( 60 FDA reports)
LETHARGY ( 59 FDA reports)
PULMONARY TUBERCULOSIS ( 59 FDA reports)
CANDIDIASIS ( 58 FDA reports)
HEPATIC STEATOSIS ( 58 FDA reports)
LEUKOCYTOSIS ( 58 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 58 FDA reports)
OSTEONECROSIS ( 58 FDA reports)
SPLENOMEGALY ( 58 FDA reports)
DRUG LEVEL INCREASED ( 57 FDA reports)
DRUG TOXICITY ( 57 FDA reports)
HEPATOTOXICITY ( 57 FDA reports)
MUSCULOSKELETAL PAIN ( 57 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 57 FDA reports)
PANCREATITIS ACUTE ( 57 FDA reports)
PNEUMONITIS ( 57 FDA reports)
PULMONARY OEDEMA ( 57 FDA reports)
THROMBOSIS ( 57 FDA reports)
HAEMATURIA ( 56 FDA reports)
HEART RATE INCREASED ( 56 FDA reports)
ILEAL STENOSIS ( 56 FDA reports)
LIVER DISORDER ( 56 FDA reports)
LUNG DISORDER ( 56 FDA reports)
LUPUS-LIKE SYNDROME ( 56 FDA reports)
DIABETIC KETOACIDOSIS ( 55 FDA reports)
DIALYSIS ( 55 FDA reports)
INTESTINAL STENOSIS ( 55 FDA reports)
MIGRAINE ( 55 FDA reports)
BLOOD BILIRUBIN INCREASED ( 54 FDA reports)
CHOLELITHIASIS ( 54 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 54 FDA reports)
SOMNOLENCE ( 54 FDA reports)
CATARACT ( 53 FDA reports)
KAPOSI'S SARCOMA ( 53 FDA reports)
METASTASES TO LIVER ( 53 FDA reports)
OEDEMA ( 53 FDA reports)
OVERDOSE ( 53 FDA reports)
BALANCE DISORDER ( 52 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 52 FDA reports)
HEART TRANSPLANT REJECTION ( 52 FDA reports)
CLOSTRIDIAL INFECTION ( 51 FDA reports)
COLONIC STENOSIS ( 51 FDA reports)
FLUSHING ( 51 FDA reports)
HAEMOPTYSIS ( 51 FDA reports)
NEPHROTIC SYNDROME ( 51 FDA reports)
SKIN ULCER ( 51 FDA reports)
T-CELL LYMPHOMA ( 51 FDA reports)
VISUAL IMPAIRMENT ( 51 FDA reports)
BACTERIAL INFECTION ( 50 FDA reports)
COLON CANCER ( 50 FDA reports)
FEELING ABNORMAL ( 50 FDA reports)
NIGHT SWEATS ( 50 FDA reports)
BREAST CANCER ( 49 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 49 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 49 FDA reports)
RASH ERYTHEMATOUS ( 49 FDA reports)
RIB FRACTURE ( 49 FDA reports)
VISUAL ACUITY REDUCED ( 49 FDA reports)
MALNUTRITION ( 48 FDA reports)
PSEUDOMONAS INFECTION ( 48 FDA reports)
HYPOKALAEMIA ( 47 FDA reports)
LIVER TRANSPLANT REJECTION ( 47 FDA reports)
NEPHROLITHIASIS ( 47 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 47 FDA reports)
ABSCESS INTESTINAL ( 46 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 46 FDA reports)
AUTOIMMUNE HEPATITIS ( 46 FDA reports)
BRONCHITIS ( 46 FDA reports)
OSTEOPOROSIS ( 46 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 46 FDA reports)
SYNCOPE ( 46 FDA reports)
TREATMENT NONCOMPLIANCE ( 46 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 45 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 45 FDA reports)
EPISTAXIS ( 45 FDA reports)
LUNG NEOPLASM ( 45 FDA reports)
LYMPHOPENIA ( 45 FDA reports)
OFF LABEL USE ( 45 FDA reports)
SKIN DISCOLOURATION ( 45 FDA reports)
ENTEROCOCCAL INFECTION ( 44 FDA reports)
HERPES SIMPLEX ( 44 FDA reports)
INFLUENZA ( 44 FDA reports)
MOBILITY DECREASED ( 44 FDA reports)
PERITONITIS ( 44 FDA reports)
RESPIRATORY DISORDER ( 44 FDA reports)
SHOCK ( 44 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 44 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 43 FDA reports)
GRAND MAL CONVULSION ( 43 FDA reports)
HEPATITIS C ( 43 FDA reports)
INJECTION SITE HAEMATOMA ( 43 FDA reports)
OROPHARYNGEAL PAIN ( 43 FDA reports)
PHARYNGITIS ( 43 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 42 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 42 FDA reports)
COMA ( 42 FDA reports)
DYSPEPSIA ( 42 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 42 FDA reports)
HYDRONEPHROSIS ( 42 FDA reports)
MULTIPLE SCLEROSIS ( 42 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 42 FDA reports)
RESPIRATORY TRACT INFECTION ( 42 FDA reports)
SURGERY ( 42 FDA reports)
BLOOD GLUCOSE INCREASED ( 41 FDA reports)
CUSHINGOID ( 41 FDA reports)
GASTROENTERITIS ( 41 FDA reports)
HODGKIN'S DISEASE ( 41 FDA reports)
INJECTION SITE PRURITUS ( 41 FDA reports)
LUNG TRANSPLANT REJECTION ( 41 FDA reports)
NECROSIS ( 41 FDA reports)
PSORIASIS ( 41 FDA reports)
SKIN EXFOLIATION ( 41 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 41 FDA reports)
APHASIA ( 40 FDA reports)
ATAXIA ( 40 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 40 FDA reports)
CARDIO-RESPIRATORY ARREST ( 40 FDA reports)
CONTUSION ( 40 FDA reports)
DIPLOPIA ( 40 FDA reports)
DYSARTHRIA ( 40 FDA reports)
HYPERGLYCAEMIA ( 40 FDA reports)
INJECTION SITE HAEMORRHAGE ( 40 FDA reports)
JC VIRUS INFECTION ( 40 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 40 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 40 FDA reports)
SWELLING ( 40 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 40 FDA reports)
AGITATION ( 39 FDA reports)
BRADYCARDIA ( 39 FDA reports)
DRUG EFFECT DECREASED ( 39 FDA reports)
ERYTHEMA NODOSUM ( 39 FDA reports)
HEPATOSPLENOMEGALY ( 39 FDA reports)
MITRAL VALVE INCOMPETENCE ( 39 FDA reports)
ABASIA ( 38 FDA reports)
BRONCHOPNEUMONIA ( 38 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 38 FDA reports)
DYSURIA ( 38 FDA reports)
ESCHERICHIA INFECTION ( 38 FDA reports)
INTESTINAL RESECTION ( 38 FDA reports)
LIVER INJURY ( 38 FDA reports)
MENTAL STATUS CHANGES ( 38 FDA reports)
MYOCARDIAL ISCHAEMIA ( 38 FDA reports)
NO THERAPEUTIC RESPONSE ( 38 FDA reports)
SKIN CANCER ( 38 FDA reports)
SPEECH DISORDER ( 38 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 37 FDA reports)
BLOOD PRESSURE DECREASED ( 37 FDA reports)
CIRCULATORY COLLAPSE ( 37 FDA reports)
CLEFT LIP AND PALATE ( 37 FDA reports)
COLONIC POLYP ( 37 FDA reports)
DRUG RESISTANCE ( 37 FDA reports)
GASTRITIS ( 37 FDA reports)
GRAFT DYSFUNCTION ( 37 FDA reports)
HEMIPARESIS ( 37 FDA reports)
MEMORY IMPAIRMENT ( 37 FDA reports)
PERICARDIAL EFFUSION ( 37 FDA reports)
PRODUCTIVE COUGH ( 37 FDA reports)
RENAL TRANSPLANT ( 37 FDA reports)
SWELLING FACE ( 37 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 37 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 36 FDA reports)
INJECTION SITE SWELLING ( 36 FDA reports)
LUNG INFECTION ( 36 FDA reports)
MASS ( 36 FDA reports)
NEOPLASM MALIGNANT ( 36 FDA reports)
NODULE ( 36 FDA reports)
OSTEOARTHRITIS ( 36 FDA reports)
PERIRECTAL ABSCESS ( 36 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 36 FDA reports)
THERAPY NON-RESPONDER ( 36 FDA reports)
DRY MOUTH ( 35 FDA reports)
DYSPNOEA EXERTIONAL ( 35 FDA reports)
FEELING HOT ( 35 FDA reports)
HEPATIC NECROSIS ( 35 FDA reports)
MENINGITIS LISTERIA ( 35 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 35 FDA reports)
PYELONEPHRITIS ( 35 FDA reports)
RECTAL ABSCESS ( 35 FDA reports)
SMALL INTESTINE CARCINOMA ( 35 FDA reports)
SUICIDE ATTEMPT ( 35 FDA reports)
ANAPHYLACTIC REACTION ( 34 FDA reports)
ARRHYTHMIA ( 34 FDA reports)
BLOOD ALBUMIN DECREASED ( 34 FDA reports)
BODY TEMPERATURE INCREASED ( 34 FDA reports)
BONE MARROW DEPRESSION ( 34 FDA reports)
BONE MARROW TOXICITY ( 34 FDA reports)
DEVICE RELATED INFECTION ( 34 FDA reports)
HAEMOLYTIC ANAEMIA ( 34 FDA reports)
HEPATIC CIRRHOSIS ( 34 FDA reports)
NEUROPATHY PERIPHERAL ( 34 FDA reports)
NEUTROPHIL COUNT DECREASED ( 34 FDA reports)
OXYGEN SATURATION DECREASED ( 34 FDA reports)
RASH MACULAR ( 34 FDA reports)
TACHYPNOEA ( 34 FDA reports)
VARICELLA ( 34 FDA reports)
ABORTION INDUCED ( 33 FDA reports)
COAGULOPATHY ( 33 FDA reports)
COLONIC OBSTRUCTION ( 33 FDA reports)
ECZEMA ( 33 FDA reports)
EPILEPSY ( 33 FDA reports)
FACE OEDEMA ( 33 FDA reports)
HEPATIC FIBROSIS ( 33 FDA reports)
HEPATOMEGALY ( 33 FDA reports)
LUPUS NEPHRITIS ( 33 FDA reports)
METASTASES TO LYMPH NODES ( 33 FDA reports)
MYOPATHY ( 33 FDA reports)
PULMONARY HYPERTENSION ( 33 FDA reports)
RASH MACULO-PAPULAR ( 33 FDA reports)
RENAL PAIN ( 33 FDA reports)
RENAL TUBULAR NECROSIS ( 33 FDA reports)
BLOOD POTASSIUM DECREASED ( 32 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 32 FDA reports)
COLECTOMY ( 32 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 32 FDA reports)
HEPATITIS B ( 32 FDA reports)
HYPONATRAEMIA ( 32 FDA reports)
INTRA-UTERINE DEATH ( 32 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 32 FDA reports)
METASTASES TO LUNG ( 32 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
UVEITIS ( 32 FDA reports)
TRANSPLANT FAILURE ( 31 FDA reports)
UROSEPSIS ( 31 FDA reports)
WEGENER'S GRANULOMATOSIS ( 31 FDA reports)
BONE PAIN ( 31 FDA reports)
ERYSIPELAS ( 31 FDA reports)
HIATUS HERNIA ( 31 FDA reports)
HYPERKALAEMIA ( 31 FDA reports)
INJECTION SITE IRRITATION ( 31 FDA reports)
INJECTION SITE REACTION ( 31 FDA reports)
PRE-ECLAMPSIA ( 31 FDA reports)
RASH PAPULAR ( 31 FDA reports)
ACUTE HEPATIC FAILURE ( 30 FDA reports)
ALVEOLITIS FIBROSING ( 30 FDA reports)
AMNESIA ( 30 FDA reports)
ATELECTASIS ( 30 FDA reports)
BLISTER ( 30 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 30 FDA reports)
MOUTH ULCERATION ( 30 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 30 FDA reports)
UNEVALUABLE EVENT ( 30 FDA reports)
URINARY INCONTINENCE ( 29 FDA reports)
CARDIAC MURMUR ( 29 FDA reports)
CEREBRAL HAEMORRHAGE ( 29 FDA reports)
CHROMATURIA ( 29 FDA reports)
DISORIENTATION ( 29 FDA reports)
DRUG INTOLERANCE ( 29 FDA reports)
FUNGAL INFECTION ( 29 FDA reports)
HYPOTONIA ( 29 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 29 FDA reports)
LEUKOENCEPHALOPATHY ( 29 FDA reports)
NERVOUS SYSTEM DISORDER ( 29 FDA reports)
NEUROTOXICITY ( 29 FDA reports)
PHOTOSENSITIVITY REACTION ( 29 FDA reports)
PULMONARY HAEMORRHAGE ( 29 FDA reports)
SERUM FERRITIN INCREASED ( 29 FDA reports)
ACTINIC KERATOSIS ( 28 FDA reports)
ACUTE RESPIRATORY FAILURE ( 28 FDA reports)
AGRANULOCYTOSIS ( 28 FDA reports)
CARDIAC DISORDER ( 28 FDA reports)
DYSSTASIA ( 28 FDA reports)
ENTEROCUTANEOUS FISTULA ( 28 FDA reports)
ILEUS ( 28 FDA reports)
METABOLIC ACIDOSIS ( 28 FDA reports)
PERICARDITIS ( 28 FDA reports)
VERTIGO ( 28 FDA reports)
APLASTIC ANAEMIA ( 27 FDA reports)
BACTERIAL SEPSIS ( 27 FDA reports)
CARDIOMEGALY ( 27 FDA reports)
DYSPHONIA ( 27 FDA reports)
EAR PAIN ( 27 FDA reports)
FAECES DISCOLOURED ( 27 FDA reports)
FIBROSIS ( 27 FDA reports)
GOUT ( 27 FDA reports)
HEMIPLEGIA ( 27 FDA reports)
HYPOGLYCAEMIA ( 27 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 27 FDA reports)
INJECTION SITE EXTRAVASATION ( 27 FDA reports)
INJURY ( 27 FDA reports)
IRON DEFICIENCY ANAEMIA ( 27 FDA reports)
LARGE INTESTINAL ULCER ( 27 FDA reports)
MUCOSAL INFLAMMATION ( 27 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 27 FDA reports)
NOCARDIOSIS ( 27 FDA reports)
PERITONITIS BACTERIAL ( 27 FDA reports)
PNEUMATOSIS INTESTINALIS ( 27 FDA reports)
SKIN DISORDER ( 27 FDA reports)
TERATOGENICITY ( 27 FDA reports)
ANAL FISSURE ( 26 FDA reports)
ANURIA ( 26 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 26 FDA reports)
DIVERTICULITIS ( 26 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 26 FDA reports)
DYSGEUSIA ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 26 FDA reports)
GASTROENTERITIS VIRAL ( 26 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 26 FDA reports)
HERPES VIRUS INFECTION ( 26 FDA reports)
HYPOKINESIA ( 26 FDA reports)
MENTAL IMPAIRMENT ( 26 FDA reports)
METASTATIC NEOPLASM ( 26 FDA reports)
MYELOFIBROSIS ( 26 FDA reports)
NOCTURIA ( 26 FDA reports)
ORTHOSTATIC HYPOTENSION ( 26 FDA reports)
PALLOR ( 26 FDA reports)
PNEUMOTHORAX ( 26 FDA reports)
PORTAL HYPERTENSION ( 26 FDA reports)
RENAL CELL CARCINOMA ( 26 FDA reports)
RHINORRHOEA ( 26 FDA reports)
SMALL FOR DATES BABY ( 26 FDA reports)
THYROID CANCER ( 26 FDA reports)
ASTHMA ( 25 FDA reports)
BLOOD CREATINE INCREASED ( 25 FDA reports)
BLOOD POTASSIUM INCREASED ( 25 FDA reports)
CUSHING'S SYNDROME ( 25 FDA reports)
ENCEPHALOPATHY ( 25 FDA reports)
GRAFT VERSUS HOST DISEASE ( 25 FDA reports)
HAEMATEMESIS ( 25 FDA reports)
LARYNGITIS ( 25 FDA reports)
NEPHRECTOMY ( 25 FDA reports)
OLIGURIA ( 25 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 25 FDA reports)
PRURITUS GENERALISED ( 25 FDA reports)
SUBCUTANEOUS ABSCESS ( 25 FDA reports)
URETERIC OBSTRUCTION ( 25 FDA reports)
VASCULITIS CEREBRAL ( 25 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 25 FDA reports)
BACTERAEMIA ( 24 FDA reports)
BLINDNESS ( 24 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 24 FDA reports)
CEREBRAL INFARCTION ( 24 FDA reports)
CHOLECYSTECTOMY ( 24 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 24 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 24 FDA reports)
DEMYELINATION ( 24 FDA reports)
HYDROCEPHALUS ( 24 FDA reports)
LIVER TRANSPLANT ( 24 FDA reports)
MULTIPLE DRUG OVERDOSE ( 24 FDA reports)
NASAL CONGESTION ( 24 FDA reports)
NEPHRITIS INTERSTITIAL ( 24 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 24 FDA reports)
RASH GENERALISED ( 24 FDA reports)
RASH PRURITIC ( 24 FDA reports)
RASH PUSTULAR ( 24 FDA reports)
SENSORY DISTURBANCE ( 24 FDA reports)
ARTHROPATHY ( 23 FDA reports)
CYSTITIS HAEMORRHAGIC ( 23 FDA reports)
FRACTURE ( 23 FDA reports)
GALLBLADDER DISORDER ( 23 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 23 FDA reports)
GRANULOMA ( 23 FDA reports)
HAEMATOMA ( 23 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 23 FDA reports)
HISTOPLASMOSIS ( 23 FDA reports)
HYPERKERATOSIS ( 23 FDA reports)
INTESTINAL FISTULA ( 23 FDA reports)
METASTASES TO BONE ( 23 FDA reports)
MYOSITIS ( 23 FDA reports)
PARVOVIRUS INFECTION ( 23 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 23 FDA reports)
PURPURA ( 23 FDA reports)
SCAR ( 23 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 23 FDA reports)
VENTRICULAR TACHYCARDIA ( 23 FDA reports)
ABDOMINAL PAIN LOWER ( 22 FDA reports)
AORTIC VALVE INCOMPETENCE ( 22 FDA reports)
BLOOD SODIUM DECREASED ( 22 FDA reports)
BREAST CYST ( 22 FDA reports)
DRUG DOSE OMISSION ( 22 FDA reports)
ECCHYMOSIS ( 22 FDA reports)
EMOTIONAL DISTRESS ( 22 FDA reports)
FLUID OVERLOAD ( 22 FDA reports)
FUNGAL ENDOCARDITIS ( 22 FDA reports)
HAEMODYNAMIC INSTABILITY ( 22 FDA reports)
HYPERLIPIDAEMIA ( 22 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 22 FDA reports)
KERATITIS HERPETIC ( 22 FDA reports)
MEDICATION ERROR ( 22 FDA reports)
METASTASIS ( 22 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 22 FDA reports)
MYCOSIS FUNGOIDES ( 22 FDA reports)
ORAL CANDIDIASIS ( 22 FDA reports)
PROSTATE CANCER ( 22 FDA reports)
SUICIDAL IDEATION ( 22 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
ADVERSE DRUG REACTION ( 21 FDA reports)
ATRIAL SEPTAL DEFECT ( 21 FDA reports)
BEHCET'S SYNDROME ( 21 FDA reports)
BRAIN OEDEMA ( 21 FDA reports)
BURNING SENSATION ( 21 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 21 FDA reports)
EOSINOPHILIA ( 21 FDA reports)
EPISCLERITIS ( 21 FDA reports)
FEBRILE NEUTROPENIA ( 21 FDA reports)
GENERALISED OEDEMA ( 21 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 21 FDA reports)
HYPERREFLEXIA ( 21 FDA reports)
HYPOALBUMINAEMIA ( 21 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 21 FDA reports)
INJECTION SITE URTICARIA ( 21 FDA reports)
KIDNEY FIBROSIS ( 21 FDA reports)
LACTIC ACIDOSIS ( 21 FDA reports)
MYASTHENIA GRAVIS ( 21 FDA reports)
MYELITIS TRANSVERSE ( 21 FDA reports)
NEOPLASM ( 21 FDA reports)
NEUTROPENIC SEPSIS ( 21 FDA reports)
OSTEONECROSIS OF JAW ( 21 FDA reports)
PELVIC PAIN ( 21 FDA reports)
PNEUMOMEDIASTINUM ( 21 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 21 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 21 FDA reports)
SKIN PAPILLOMA ( 21 FDA reports)
SPINAL COMPRESSION FRACTURE ( 21 FDA reports)
VARICES OESOPHAGEAL ( 21 FDA reports)
VISUAL DISTURBANCE ( 21 FDA reports)
URINARY RETENTION ( 20 FDA reports)
ABDOMINAL TENDERNESS ( 20 FDA reports)
AGGRESSION ( 20 FDA reports)
APHTHOUS STOMATITIS ( 20 FDA reports)
CARDIOMYOPATHY ( 20 FDA reports)
CERVIX CARCINOMA ( 20 FDA reports)
CHOLECYSTITIS ( 20 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 20 FDA reports)
DIFFICULTY IN WALKING ( 20 FDA reports)
ENDOCARDITIS ( 20 FDA reports)
FELTY'S SYNDROME ( 20 FDA reports)
FISTULA DISCHARGE ( 20 FDA reports)
FUNGAL PERITONITIS ( 20 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 20 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 20 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 20 FDA reports)
INJECTION SITE NODULE ( 20 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 20 FDA reports)
LABORATORY TEST ABNORMAL ( 20 FDA reports)
LUNG NEOPLASM MALIGNANT ( 20 FDA reports)
MICROANGIOPATHY ( 20 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 20 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 20 FDA reports)
PLATELET DISORDER ( 20 FDA reports)
POLYP ( 20 FDA reports)
SINUS HEADACHE ( 20 FDA reports)
SKIN NODULE ( 20 FDA reports)
SKIN TIGHTNESS ( 20 FDA reports)
TENDERNESS ( 20 FDA reports)
ANGINA PECTORIS ( 19 FDA reports)
BLOOD CALCIUM DECREASED ( 19 FDA reports)
BRAIN STEM SYNDROME ( 19 FDA reports)
CANDIDA SEPSIS ( 19 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 19 FDA reports)
COGNITIVE DISORDER ( 19 FDA reports)
CYST ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
DYSKINESIA ( 19 FDA reports)
EJECTION FRACTION DECREASED ( 19 FDA reports)
ESCHERICHIA SEPSIS ( 19 FDA reports)
EYE SWELLING ( 19 FDA reports)
FEMUR FRACTURE ( 19 FDA reports)
FLUID RETENTION ( 19 FDA reports)
FUNGAL SKIN INFECTION ( 19 FDA reports)
GASTROINTESTINAL ULCER ( 19 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 19 FDA reports)
ILL-DEFINED DISORDER ( 19 FDA reports)
INJECTION SITE WARMTH ( 19 FDA reports)
LOBAR PNEUMONIA ( 19 FDA reports)
MENINGITIS ASEPTIC ( 19 FDA reports)
NYSTAGMUS ( 19 FDA reports)
OPTIC NEURITIS ( 19 FDA reports)
PEMPHIGUS ( 19 FDA reports)
PLEURAL FIBROSIS ( 19 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 19 FDA reports)
PRESYNCOPE ( 19 FDA reports)
RALES ( 19 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 19 FDA reports)
SENSORY LOSS ( 19 FDA reports)
SINUS TACHYCARDIA ( 19 FDA reports)
STOMATITIS ( 19 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 19 FDA reports)
TRIGGER FINGER ( 18 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 18 FDA reports)
WHIPPLE'S DISEASE ( 18 FDA reports)
BRONCHOSPASM ( 18 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 18 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 18 FDA reports)
CORONARY ARTERY STENOSIS ( 18 FDA reports)
DRY SKIN ( 18 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 18 FDA reports)
GASTRIC ULCER ( 18 FDA reports)
HALLUCINATION ( 18 FDA reports)
HYPERTONIC BLADDER ( 18 FDA reports)
ISCHAEMIC STROKE ( 18 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 18 FDA reports)
LOCALISED INFECTION ( 18 FDA reports)
MELAENA ( 18 FDA reports)
MELANOCYTIC NAEVUS ( 18 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 18 FDA reports)
NEUTROPHIL COUNT INCREASED ( 18 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 18 FDA reports)
OESOPHAGITIS ( 18 FDA reports)
PAPILLOEDEMA ( 18 FDA reports)
PHOTOPHOBIA ( 18 FDA reports)
PLATELET COUNT INCREASED ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
SKIN INDURATION ( 18 FDA reports)
SLEEP DISORDER ( 18 FDA reports)
SUBILEUS ( 18 FDA reports)
ABDOMINAL MASS ( 17 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 17 FDA reports)
ADENOCARCINOMA ( 17 FDA reports)
BLINDNESS UNILATERAL ( 17 FDA reports)
BRAIN ABSCESS ( 17 FDA reports)
CAROTID ARTERY STENOSIS ( 17 FDA reports)
CEREBRAL ISCHAEMIA ( 17 FDA reports)
CHEST X-RAY ABNORMAL ( 17 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 17 FDA reports)
CORONARY ARTERY OCCLUSION ( 17 FDA reports)
CYANOSIS ( 17 FDA reports)
CYTOLYTIC HEPATITIS ( 17 FDA reports)
DERMATITIS ( 17 FDA reports)
EYE INFLAMMATION ( 17 FDA reports)
FOLLICULITIS ( 17 FDA reports)
ILEOSTOMY ( 17 FDA reports)
IMMUNOGLOBULINS DECREASED ( 17 FDA reports)
JOINT STIFFNESS ( 17 FDA reports)
KLEBSIELLA INFECTION ( 17 FDA reports)
LARYNGITIS VIRAL ( 17 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 17 FDA reports)
MOUTH INJURY ( 17 FDA reports)
MOVEMENT DISORDER ( 17 FDA reports)
PANIC ATTACK ( 17 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 17 FDA reports)
PNEUMONIA FUNGAL ( 17 FDA reports)
PROSTATITIS ( 17 FDA reports)
RECTAL CANCER ( 17 FDA reports)
RECTAL DISCHARGE ( 17 FDA reports)
SARCOIDOSIS ( 17 FDA reports)
SKIN HYPERPIGMENTATION ( 17 FDA reports)
SUDDEN DEATH ( 17 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 17 FDA reports)
ULCER ( 17 FDA reports)
VIRAL PHARYNGITIS ( 17 FDA reports)
WOUND ( 17 FDA reports)
TOOTHACHE ( 16 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 16 FDA reports)
TUMOUR LYSIS SYNDROME ( 16 FDA reports)
UBIQUINONE DECREASED ( 16 FDA reports)
ABDOMINAL ADHESIONS ( 16 FDA reports)
ABDOMINAL INFECTION ( 16 FDA reports)
ACUTE CORONARY SYNDROME ( 16 FDA reports)
ADVERSE EVENT ( 16 FDA reports)
ARTERIOSCLEROSIS ( 16 FDA reports)
AZOTAEMIA ( 16 FDA reports)
BLOOD URIC ACID INCREASED ( 16 FDA reports)
BONE DENSITY DECREASED ( 16 FDA reports)
BURKITT'S LYMPHOMA ( 16 FDA reports)
CARDIAC VALVE VEGETATION ( 16 FDA reports)
CHRONIC SINUSITIS ( 16 FDA reports)
CONJUNCTIVITIS ( 16 FDA reports)
DELIRIUM ( 16 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 16 FDA reports)
FLANK PAIN ( 16 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
HAEMANGIOMA CONGENITAL ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
HEPATIC ENCEPHALOPATHY ( 16 FDA reports)
HYPERBILIRUBINAEMIA ( 16 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 16 FDA reports)
IMMUNE SYSTEM DISORDER ( 16 FDA reports)
IMMUNODEFICIENCY ( 16 FDA reports)
MENTAL DISORDER ( 16 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 16 FDA reports)
NORMAL NEWBORN ( 16 FDA reports)
ORCHITIS ( 16 FDA reports)
PETECHIAE ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
PNEUMONIA LEGIONELLA ( 16 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 16 FDA reports)
RESTLESSNESS ( 16 FDA reports)
SALMONELLOSIS ( 16 FDA reports)
SINUS POLYP ( 16 FDA reports)
SUBCUTANEOUS NODULE ( 16 FDA reports)
TENDON RUPTURE ( 16 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
ACNE ( 15 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
BRONCHOSTENOSIS ( 15 FDA reports)
CREPITATIONS ( 15 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 15 FDA reports)
DEVELOPMENTAL DELAY ( 15 FDA reports)
DRUG ERUPTION ( 15 FDA reports)
GINGIVAL HYPERPLASIA ( 15 FDA reports)
HIP FRACTURE ( 15 FDA reports)
HOT FLUSH ( 15 FDA reports)
HYSTERECTOMY ( 15 FDA reports)
ILEAL PERFORATION ( 15 FDA reports)
JOINT EFFUSION ( 15 FDA reports)
KERATITIS ( 15 FDA reports)
LISTERIOSIS ( 15 FDA reports)
LOCAL SWELLING ( 15 FDA reports)
LUNG ABSCESS ( 15 FDA reports)
LUNG ADENOCARCINOMA ( 15 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 15 FDA reports)
MUSCLE TIGHTNESS ( 15 FDA reports)
NEPHRITIS ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 15 FDA reports)
OTITIS MEDIA ( 15 FDA reports)
PERSONALITY CHANGE ( 15 FDA reports)
POLLAKIURIA ( 15 FDA reports)
PREMATURE DELIVERY ( 15 FDA reports)
RENAL CANCER ( 15 FDA reports)
RENAL GRAFT LOSS ( 15 FDA reports)
RESPIRATORY RATE INCREASED ( 15 FDA reports)
SERUM SICKNESS ( 15 FDA reports)
SKIN PLAQUE ( 15 FDA reports)
SPLENECTOMY ( 15 FDA reports)
STREPTOCOCCAL INFECTION ( 15 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 15 FDA reports)
TREATMENT FAILURE ( 15 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 15 FDA reports)
WHEEZING ( 15 FDA reports)
WOUND DEHISCENCE ( 15 FDA reports)
TOOTH INFECTION ( 14 FDA reports)
WOUND INFECTION ( 14 FDA reports)
ACIDOSIS ( 14 FDA reports)
ACINETOBACTER INFECTION ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 14 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 14 FDA reports)
BLOOD GLUCOSE DECREASED ( 14 FDA reports)
CACHEXIA ( 14 FDA reports)
CATHETER RELATED INFECTION ( 14 FDA reports)
CEREBRAL ATROPHY ( 14 FDA reports)
CHORIORETINOPATHY ( 14 FDA reports)
COLON CANCER METASTATIC ( 14 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 14 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 14 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 14 FDA reports)
DYSPLASIA ( 14 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 14 FDA reports)
ERYTHEMA INFECTIOSUM ( 14 FDA reports)
FUNGAEMIA ( 14 FDA reports)
GASTROINTESTINAL INFECTION ( 14 FDA reports)
GRAFT COMPLICATION ( 14 FDA reports)
HAEMOLYSIS ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
IMPAIRED WORK ABILITY ( 14 FDA reports)
INTESTINAL ISCHAEMIA ( 14 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 14 FDA reports)
MUSCLE TWITCHING ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
NON-CARDIAC CHEST PAIN ( 14 FDA reports)
OSTEOPENIA ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 14 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 14 FDA reports)
PULMONARY CONGESTION ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RAYNAUD'S PHENOMENON ( 14 FDA reports)
RENAL TUBULAR DISORDER ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
SEROTONIN SYNDROME ( 14 FDA reports)
SINUS DISORDER ( 14 FDA reports)
SMALL INTESTINAL PERFORATION ( 14 FDA reports)
STRABISMUS ( 14 FDA reports)
STRESS ( 14 FDA reports)
THIRST ( 14 FDA reports)
TINNITUS ( 14 FDA reports)
ABORTION MISSED ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 13 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ANAPHYLACTIC SHOCK ( 13 FDA reports)
ANGIOPATHY ( 13 FDA reports)
BILE DUCT CANCER ( 13 FDA reports)
BLOOD AMYLASE INCREASED ( 13 FDA reports)
BONE DISORDER ( 13 FDA reports)
BREAST CANCER FEMALE ( 13 FDA reports)
CARDIOVASCULAR DISORDER ( 13 FDA reports)
CHOLANGITIS ( 13 FDA reports)
CHOLECYSTITIS ACUTE ( 13 FDA reports)
CHOLESTASIS OF PREGNANCY ( 13 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 13 FDA reports)
DEAFNESS ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
EYE DISORDER ( 13 FDA reports)
EYE PAIN ( 13 FDA reports)
FEELING COLD ( 13 FDA reports)
FOETAL DISTRESS SYNDROME ( 13 FDA reports)
FURUNCLE ( 13 FDA reports)
GASTRIC CANCER ( 13 FDA reports)
GASTRIC DISORDER ( 13 FDA reports)
GLOMERULONEPHRITIS ( 13 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 13 FDA reports)
HAEMANGIOMA OF LIVER ( 13 FDA reports)
HEARING IMPAIRED ( 13 FDA reports)
HEPATIC HAEMATOMA ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 13 FDA reports)
INJECTION SITE RASH ( 13 FDA reports)
INTESTINAL ULCER ( 13 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 13 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 13 FDA reports)
MENORRHAGIA ( 13 FDA reports)
MULTIPLE MYELOMA ( 13 FDA reports)
MUSCLE ATROPHY ( 13 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 13 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 13 FDA reports)
OLIGOHYDRAMNIOS ( 13 FDA reports)
OPPORTUNISTIC INFECTION ( 13 FDA reports)
ORAL PAIN ( 13 FDA reports)
PAIN IN JAW ( 13 FDA reports)
PARTIAL SEIZURES ( 13 FDA reports)
PELVIC ABSCESS ( 13 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 13 FDA reports)
PERITONEAL TUBERCULOSIS ( 13 FDA reports)
PLEURITIC PAIN ( 13 FDA reports)
PNEUMOPERITONEUM ( 13 FDA reports)
PORTAL VEIN THROMBOSIS ( 13 FDA reports)
PROCTITIS ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
PULMONARY VASCULITIS ( 13 FDA reports)
RENAL TUBULAR ATROPHY ( 13 FDA reports)
SCAB ( 13 FDA reports)
SKIN HYPERTROPHY ( 13 FDA reports)
STENOTROPHOMONAS INFECTION ( 13 FDA reports)
STILLBIRTH ( 13 FDA reports)
SYNOVITIS ( 13 FDA reports)
THROAT TIGHTNESS ( 13 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 13 FDA reports)
URINE OUTPUT DECREASED ( 13 FDA reports)
UTERINE LEIOMYOMA ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 13 FDA reports)
WRIST FRACTURE ( 13 FDA reports)
VENOUS THROMBOSIS ( 12 FDA reports)
WOUND SECRETION ( 12 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 12 FDA reports)
APPENDICITIS ( 12 FDA reports)
ASPIRATION ( 12 FDA reports)
BILE DUCT OBSTRUCTION ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 12 FDA reports)
BLOOD MAGNESIUM DECREASED ( 12 FDA reports)
BRONCHIAL CARCINOMA ( 12 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX SEPSIS ( 12 FDA reports)
CARDIOGENIC SHOCK ( 12 FDA reports)
CERVICAL DYSPLASIA ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
EUPHORIC MOOD ( 12 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 12 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 12 FDA reports)
FAECALOMA ( 12 FDA reports)
FIBRIN D DIMER INCREASED ( 12 FDA reports)
GASTROINTESTINAL NECROSIS ( 12 FDA reports)
GRAFT LOSS ( 12 FDA reports)
HAEMORRHOIDS ( 12 FDA reports)
HIRSUTISM ( 12 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 12 FDA reports)
HYPERCHOLESTEROLAEMIA ( 12 FDA reports)
HYPOMAGNESAEMIA ( 12 FDA reports)
HYPOTHYROIDISM ( 12 FDA reports)
IATROGENIC INJURY ( 12 FDA reports)
ILEAL FISTULA ( 12 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 12 FDA reports)
LIP SWELLING ( 12 FDA reports)
MACULAR OEDEMA ( 12 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 12 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
NEOPLASM RECURRENCE ( 12 FDA reports)
NEPHROPATHY ( 12 FDA reports)
NO ADVERSE EVENT ( 12 FDA reports)
ODYNOPHAGIA ( 12 FDA reports)
ORAL DISORDER ( 12 FDA reports)
ORGANISING PNEUMONIA ( 12 FDA reports)
PERIPHERAL COLDNESS ( 12 FDA reports)
PERITONEAL CANDIDIASIS ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
PLASMACYTOMA ( 12 FDA reports)
PNEUMONIA ASPIRATION ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PROCEDURAL COMPLICATION ( 12 FDA reports)
PROTEIN TOTAL DECREASED ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
RESPIRATORY TRACT CONGESTION ( 12 FDA reports)
RHINITIS ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 12 FDA reports)
THROAT IRRITATION ( 12 FDA reports)
ABORTION ( 11 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 11 FDA reports)
ANAPHYLACTOID REACTION ( 11 FDA reports)
ANORECTAL DISORDER ( 11 FDA reports)
ARTHROPOD BITE ( 11 FDA reports)
ATRIAL FLUTTER ( 11 FDA reports)
AUTOIMMUNE DISORDER ( 11 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 11 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 11 FDA reports)
BIOPSY LIVER ABNORMAL ( 11 FDA reports)
BK VIRUS INFECTION ( 11 FDA reports)
BLADDER CANCER ( 11 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CRYING ( 11 FDA reports)
CSF PROTEIN INCREASED ( 11 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 11 FDA reports)
DERMATITIS ALLERGIC ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
DIVERTICULUM ( 11 FDA reports)
DRUG PRESCRIBING ERROR ( 11 FDA reports)
DYSPHASIA ( 11 FDA reports)
ECTOPIC PREGNANCY ( 11 FDA reports)
EMPYEMA ( 11 FDA reports)
ENCEPHALITIS VIRAL ( 11 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 11 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 11 FDA reports)
GASTROINTESTINAL CARCINOMA ( 11 FDA reports)
GINGIVAL BLEEDING ( 11 FDA reports)
GROWTH RETARDATION ( 11 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 11 FDA reports)
HYPERSOMNIA ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
HYPERURICAEMIA ( 11 FDA reports)
HYPOCALCAEMIA ( 11 FDA reports)
ILEITIS ( 11 FDA reports)
ILEUS PARALYTIC ( 11 FDA reports)
INFECTIOUS PERITONITIS ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
LAPAROTOMY ( 11 FDA reports)
LEIOMYOSARCOMA ( 11 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 11 FDA reports)
LIMB DISCOMFORT ( 11 FDA reports)
LYMPHADENITIS ( 11 FDA reports)
LYMPHOCELE ( 11 FDA reports)
MALIGNANT TUMOUR EXCISION ( 11 FDA reports)
MENINGIOMA ( 11 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 11 FDA reports)
MUSCLE CRAMP ( 11 FDA reports)
NEPHROSCLEROSIS ( 11 FDA reports)
NEUROLOGICAL SYMPTOM ( 11 FDA reports)
NEUTROPHILIA ( 11 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 11 FDA reports)
PANNICULITIS ( 11 FDA reports)
PERIPHERAL ISCHAEMIA ( 11 FDA reports)
PLATELET COUNT ABNORMAL ( 11 FDA reports)
PNEUMONIA ASPERGILLUS ( 11 FDA reports)
POLYMYOSITIS ( 11 FDA reports)
PROTEIN URINE PRESENT ( 11 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 11 FDA reports)
PUSTULAR PSORIASIS ( 11 FDA reports)
PYODERMA GANGRENOSUM ( 11 FDA reports)
RECTAL ULCER ( 11 FDA reports)
RED BLOOD CELL ABNORMALITY ( 11 FDA reports)
RETCHING ( 11 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 11 FDA reports)
RIGHT VENTRICULAR FAILURE ( 11 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
STRONGYLOIDIASIS ( 11 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 11 FDA reports)
SWOLLEN TONGUE ( 11 FDA reports)
SYNDACTYLY ( 11 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 11 FDA reports)
UNINTENDED PREGNANCY ( 11 FDA reports)
TYPE 1 DIABETES MELLITUS ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 10 FDA reports)
UTERINE CANCER ( 10 FDA reports)
VAGINAL HAEMORRHAGE ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ANAL STENOSIS ( 10 FDA reports)
AORTIC DISSECTION ( 10 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 10 FDA reports)
ARTHRITIS INFECTIVE ( 10 FDA reports)
BILIARY DILATATION ( 10 FDA reports)
BONE MARROW DISORDER ( 10 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 10 FDA reports)
CHOLECYSTITIS CHRONIC ( 10 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
COCCIDIOIDOMYCOSIS ( 10 FDA reports)
COLECTOMY TOTAL ( 10 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 10 FDA reports)
CONGENITAL ANOMALY ( 10 FDA reports)
CRYPTOCOCCOSIS ( 10 FDA reports)
DEVICE RELATED SEPSIS ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
DYSTONIA ( 10 FDA reports)
EMOTIONAL DISORDER ( 10 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
FEMORAL NECK FRACTURE ( 10 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 10 FDA reports)
FOOT FRACTURE ( 10 FDA reports)
GASTROINTESTINAL TOXICITY ( 10 FDA reports)
GINGIVAL HYPERTROPHY ( 10 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 10 FDA reports)
HEAD INJURY ( 10 FDA reports)
HEPATIC NEOPLASM ( 10 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 10 FDA reports)
HUMAN EHRLICHIOSIS ( 10 FDA reports)
HYPERPARATHYROIDISM ( 10 FDA reports)
HYPERTHERMIA ( 10 FDA reports)
HYPERTHYROIDISM ( 10 FDA reports)
ILEAL ULCER ( 10 FDA reports)
ILEOSTOMY CLOSURE ( 10 FDA reports)
IMPETIGO ( 10 FDA reports)
INCISION SITE INFECTION ( 10 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 10 FDA reports)
INFERTILITY ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 10 FDA reports)
INTESTINAL HAEMORRHAGE ( 10 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 10 FDA reports)
IRON DEFICIENCY ( 10 FDA reports)
ISCHAEMIA ( 10 FDA reports)
KIDNEY INFECTION ( 10 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 10 FDA reports)
LIPASE INCREASED ( 10 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 10 FDA reports)
LUNG CONSOLIDATION ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
MARROW HYPERPLASIA ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 10 FDA reports)
MONOPARESIS ( 10 FDA reports)
MUCORMYCOSIS ( 10 FDA reports)
NEUROMYELITIS OPTICA ( 10 FDA reports)
OCULAR HYPERAEMIA ( 10 FDA reports)
OESOPHAGEAL ATRESIA ( 10 FDA reports)
OPEN WOUND ( 10 FDA reports)
ORAL HERPES ( 10 FDA reports)
PO2 DECREASED ( 10 FDA reports)
POLYARTHRITIS ( 10 FDA reports)
POST PROCEDURAL INFECTION ( 10 FDA reports)
PROCTALGIA ( 10 FDA reports)
PSEUDOMONAL SEPSIS ( 10 FDA reports)
PULMONARY NECROSIS ( 10 FDA reports)
RETINAL VASCULITIS ( 10 FDA reports)
ROTATOR CUFF SYNDROME ( 10 FDA reports)
SJOGREN'S SYNDROME ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
TOOTH EXTRACTION ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 9 FDA reports)
ACTINOMYCOSIS ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 9 FDA reports)
ALBUMINURIA ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 9 FDA reports)
BRAIN NEOPLASM ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CARDIAC MYXOMA ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 9 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 9 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DEAFNESS NEUROSENSORY ( 9 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DIABETIC NEUROPATHY ( 9 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 9 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 9 FDA reports)
ELECTROLYTE IMBALANCE ( 9 FDA reports)
EOSINOPHILIC PNEUMONIA ( 9 FDA reports)
ERYTHEMA MULTIFORME ( 9 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 9 FDA reports)
EYE INFECTION FUNGAL ( 9 FDA reports)
EYE MOVEMENT DISORDER ( 9 FDA reports)
FACIAL PALSY ( 9 FDA reports)
FIBROMYALGIA ( 9 FDA reports)
GAMMOPATHY ( 9 FDA reports)
GASTRIC HAEMORRHAGE ( 9 FDA reports)
GASTROINTESTINAL FISTULA ( 9 FDA reports)
GENERALISED ANXIETY DISORDER ( 9 FDA reports)
GINGIVAL PAIN ( 9 FDA reports)
GLOMERULOSCLEROSIS ( 9 FDA reports)
GRANULOCYTOPENIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
HYPOPROTEINAEMIA ( 9 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
INTESTINAL MASS ( 9 FDA reports)
INTESTINAL OPERATION ( 9 FDA reports)
IRRITABILITY ( 9 FDA reports)
LEG AMPUTATION ( 9 FDA reports)
LIPOMATOSIS ( 9 FDA reports)
LUNG CANCER METASTATIC ( 9 FDA reports)
LYMPH NODE PAIN ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
MECHANICAL VENTILATION ( 9 FDA reports)
MENINGITIS VIRAL ( 9 FDA reports)
METAPLASIA ( 9 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 9 FDA reports)
MICROTIA ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MULTI-ORGAN DISORDER ( 9 FDA reports)
NASAL CYST ( 9 FDA reports)
NASAL DISORDER ( 9 FDA reports)
NEONATAL ASPHYXIA ( 9 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 9 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 9 FDA reports)
OESOPHAGEAL PAIN ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
OVARIAN CANCER METASTATIC ( 9 FDA reports)
PARKINSONISM ( 9 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PELVIC FRACTURE ( 9 FDA reports)
PEMPHIGOID ( 9 FDA reports)
PERITONITIS SCLEROSING ( 9 FDA reports)
PLASMABLASTIC LYMPHOMA ( 9 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
PULMONARY TOXICITY ( 9 FDA reports)
RETINAL DETACHMENT ( 9 FDA reports)
SENSATION OF PRESSURE ( 9 FDA reports)
SINUS RHYTHM ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
SKIN NEOPLASM EXCISION ( 9 FDA reports)
SMALL INTESTINAL STENOSIS ( 9 FDA reports)
SPIROMETRY ABNORMAL ( 9 FDA reports)
SUBDURAL HAEMATOMA ( 9 FDA reports)
THROMBOCYTHAEMIA ( 9 FDA reports)
TRICHOSPORON INFECTION ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
URETERIC STENOSIS ( 9 FDA reports)
VENTRICULAR HYPERTROPHY ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
TRANSFUSION ( 8 FDA reports)
TRANSFUSION REACTION ( 8 FDA reports)
UPPER LIMB FRACTURE ( 8 FDA reports)
URINE ANALYSIS ABNORMAL ( 8 FDA reports)
VENA CAVA THROMBOSIS ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
WHEELCHAIR USER ( 8 FDA reports)
ZYGOMYCOSIS ( 8 FDA reports)
ACCIDENTAL NEEDLE STICK ( 8 FDA reports)
ALKALOSIS ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 8 FDA reports)
ANASTOMOTIC COMPLICATION ( 8 FDA reports)
AREFLEXIA ( 8 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 8 FDA reports)
ATRIAL TACHYCARDIA ( 8 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 8 FDA reports)
BLOOD CHLORIDE INCREASED ( 8 FDA reports)
BLOOD HIV RNA INCREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BONE MARROW TRANSPLANT ( 8 FDA reports)
BOWEN'S DISEASE ( 8 FDA reports)
BRAIN STEM INFARCTION ( 8 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 8 FDA reports)
BURKITT'S LYMPHOMA STAGE III ( 8 FDA reports)
BURSITIS ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CARPAL TUNNEL SYNDROME ( 8 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 8 FDA reports)
CHOLANGITIS CHRONIC ( 8 FDA reports)
CHOLANGITIS SCLEROSING ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 8 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 8 FDA reports)
CYSTITIS ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DERMATITIS PSORIASIFORM ( 8 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 8 FDA reports)
DNA ANTIBODY POSITIVE ( 8 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 8 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
DUODENITIS ( 8 FDA reports)
DYSAESTHESIA ( 8 FDA reports)
EAR INFECTION ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
ENCEPHALITIS HERPES ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
FUNGAL SEPSIS ( 8 FDA reports)
GANGLIONEUROMA ( 8 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 8 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HEPATITIS E ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HEPATOCELLULAR INJURY ( 8 FDA reports)
HEPATORENAL FAILURE ( 8 FDA reports)
HORMONE LEVEL ABNORMAL ( 8 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 8 FDA reports)
HYPERTELORISM OF ORBIT ( 8 FDA reports)
HYPERTRICHOSIS ( 8 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 8 FDA reports)
INJECTION SITE BRUISING ( 8 FDA reports)
INJECTION SITE INDURATION ( 8 FDA reports)
INJECTION SITE ULCER ( 8 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 8 FDA reports)
JAW DISORDER ( 8 FDA reports)
LIMB INJURY ( 8 FDA reports)
LUNG TRANSPLANT ( 8 FDA reports)
LYMPH NODE TUBERCULOSIS ( 8 FDA reports)
LYMPHOHISTIOCYTOSIS ( 8 FDA reports)
LYMPHOMATOID PAPULOSIS ( 8 FDA reports)
MAJOR DEPRESSION ( 8 FDA reports)
MENINGEAL DISORDER ( 8 FDA reports)
MENINGITIS TUBERCULOUS ( 8 FDA reports)
MENSTRUAL DISORDER ( 8 FDA reports)
METASTASES TO PERITONEUM ( 8 FDA reports)
MICROGNATHIA ( 8 FDA reports)
MONOCYTE COUNT INCREASED ( 8 FDA reports)
MULTIPLE CARDIAC DEFECTS ( 8 FDA reports)
MULTIPLE FRACTURES ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
NAIL DISCOLOURATION ( 8 FDA reports)
NECROTISING FASCIITIS ( 8 FDA reports)
NEONATAL ASPIRATION ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PEAU D'ORANGE ( 8 FDA reports)
PERITONEAL ABSCESS ( 8 FDA reports)
PERITONSILLITIS ( 8 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POST HERPETIC NEURALGIA ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
POTENTIATING DRUG INTERACTION ( 8 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 8 FDA reports)
PROCTOCOLECTOMY ( 8 FDA reports)
PULMONARY ARTERY DILATATION ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
RENAL MASS ( 8 FDA reports)
RETICULOCYTE COUNT INCREASED ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
STEM CELL TRANSPLANT ( 8 FDA reports)
STOMACH DISCOMFORT ( 8 FDA reports)
SURGICAL PROCEDURE REPEATED ( 8 FDA reports)
SYNCOPE VASOVAGAL ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
ADHESION ( 7 FDA reports)
AGEUSIA ( 7 FDA reports)
ALTERNARIA INFECTION ( 7 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 7 FDA reports)
ANAL CANCER ( 7 FDA reports)
ANASTOMOTIC LEAK ( 7 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 7 FDA reports)
APLASIA ( 7 FDA reports)
APPENDICITIS PERFORATED ( 7 FDA reports)
ARTHRITIS BACTERIAL ( 7 FDA reports)
AUTISM ( 7 FDA reports)
BILIARY TRACT DISORDER ( 7 FDA reports)
BLOOD CALCIUM INCREASED ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 7 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 7 FDA reports)
BRACHYCEPHALY ( 7 FDA reports)
CAMPTODACTYLY CONGENITAL ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 7 FDA reports)
CEREBRAL ASPERGILLOSIS ( 7 FDA reports)
COLD SWEAT ( 7 FDA reports)
COLOBOMA ( 7 FDA reports)
COLONIC FISTULA ( 7 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 7 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 7 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 7 FDA reports)
ENDOTRACHEAL INTUBATION ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
ENTEROCOCCAL SEPSIS ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EYE INFECTION ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 7 FDA reports)
FOETAL DISORDER ( 7 FDA reports)
GASTROINTESTINAL OEDEMA ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 7 FDA reports)
HAEMANGIOMA ( 7 FDA reports)
HAEMORRHAGIC ANAEMIA ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HEAD TITUBATION ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HERPES OESOPHAGITIS ( 7 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPEROSMOLAR STATE ( 7 FDA reports)
HYPERPYREXIA ( 7 FDA reports)
HYPOREFLEXIA ( 7 FDA reports)
HYPOVOLAEMIA ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INJECTION SITE BURNING ( 7 FDA reports)
INJECTION SITE CELLULITIS ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
JOINT DISLOCATION ( 7 FDA reports)
JOINT SURGERY ( 7 FDA reports)
LACRIMATION INCREASED ( 7 FDA reports)
LARYNGEAL CANCER ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
LEFT VENTRICULAR FAILURE ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LIVER ABSCESS ( 7 FDA reports)
LIVER TENDERNESS ( 7 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
MUSCLE RUPTURE ( 7 FDA reports)
MYCOBACTERIAL INFECTION ( 7 FDA reports)
MYOCARDITIS ( 7 FDA reports)
NAIL DISORDER ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NASAL SEPTUM DISORDER ( 7 FDA reports)
NEPHROSTOMY ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 7 FDA reports)
ORAL DISCOMFORT ( 7 FDA reports)
ORTHOPNOEA ( 7 FDA reports)
OVARIAN FAILURE ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PANNICULITIS LOBULAR ( 7 FDA reports)
PARAPARESIS ( 7 FDA reports)
PARESIS ( 7 FDA reports)
PAST-POINTING ( 7 FDA reports)
PERIORBITAL OEDEMA ( 7 FDA reports)
PERONEAL NERVE PALSY ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
POLYSEROSITIS ( 7 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 7 FDA reports)
PRURIGO ( 7 FDA reports)
PULMONARY SARCOIDOSIS ( 7 FDA reports)
PULSE ABSENT ( 7 FDA reports)
RADIATION SKIN INJURY ( 7 FDA reports)
RADIOTHERAPY ( 7 FDA reports)
REBOUND EFFECT ( 7 FDA reports)
RENAL CYST ( 7 FDA reports)
RHEUMATOID NODULE ( 7 FDA reports)
RHEUMATOID VASCULITIS ( 7 FDA reports)
SCEDOSPORIUM INFECTION ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SENSATION OF HEAVINESS ( 7 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 7 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 7 FDA reports)
SOFT TISSUE DISORDER ( 7 FDA reports)
SPINAL CORD COMPRESSION ( 7 FDA reports)
SPINAL DISORDER ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
SUBDURAL HAEMORRHAGE ( 7 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
SYSTEMIC MYCOSIS ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
TIC ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
VITREOUS HAEMORRHAGE ( 7 FDA reports)
WALKING AID USER ( 7 FDA reports)
WOUND COMPLICATION ( 7 FDA reports)
YELLOW SKIN ( 7 FDA reports)
TOOTH HYPOPLASIA ( 6 FDA reports)
TRACHEOBRONCHITIS ( 6 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
URETERITIS ( 6 FDA reports)
VASCULAR GRAFT COMPLICATION ( 6 FDA reports)
VASCULITIS NECROTISING ( 6 FDA reports)
VIRAL DNA TEST POSITIVE ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
WEIGHT BEARING DIFFICULTY ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABDOMINAL OPERATION ( 6 FDA reports)
ABDOMINAL WALL INFECTION ( 6 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ACUTE ABDOMEN ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
ACUTE LEUKAEMIA ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 6 FDA reports)
ANGIONEUROTIC OEDEMA ( 6 FDA reports)
ANGIOSARCOMA ( 6 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 6 FDA reports)
ANTITHROMBIN III DECREASED ( 6 FDA reports)
APATHY ( 6 FDA reports)
APNOEA ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 6 FDA reports)
AUTOANTIBODY POSITIVE ( 6 FDA reports)
BEDRIDDEN ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 6 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 6 FDA reports)
BLOOD LACTIC ACID INCREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BONE LESION ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CARDIOTOXICITY ( 6 FDA reports)
CARNITINE DECREASED ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CEREBELLAR ATROPHY ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CHOLESTATIC LIVER INJURY ( 6 FDA reports)
CHOREA ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
CLAVICLE FRACTURE ( 6 FDA reports)
CLINODACTYLY ( 6 FDA reports)
COGWHEEL RIGIDITY ( 6 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 6 FDA reports)
COR PULMONALE ( 6 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 6 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
CUTANEOUS VASCULITIS ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSLIPIDAEMIA ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EMBOLISM ( 6 FDA reports)
ENDOMETRIAL CANCER ( 6 FDA reports)
ENTEROVESICAL FISTULA ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
ESCHERICHIA TEST POSITIVE ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EXTRADURAL ABSCESS ( 6 FDA reports)
EYE INFECTION BACTERIAL ( 6 FDA reports)
FACIAL PAIN ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
FOETAL DEATH ( 6 FDA reports)
FOOD INTERACTION ( 6 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 6 FDA reports)
GALLBLADDER NECROSIS ( 6 FDA reports)
GALLBLADDER OPERATION ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 6 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GASTROINTESTINAL PERFORATION ( 6 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 6 FDA reports)
GASTROINTESTINAL STENOSIS ( 6 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 6 FDA reports)
GRANULOMA SKIN ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 6 FDA reports)
HYPOCOAGULABLE STATE ( 6 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 6 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
INDUCED LABOUR ( 6 FDA reports)
INGUINAL HERNIA ( 6 FDA reports)
INJECTION SITE OEDEMA ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
LACERATION ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LARGE INTESTINAL STRICTURE ( 6 FDA reports)
LATENT TUBERCULOSIS ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
MACROCYTOSIS ( 6 FDA reports)
MEAN CELL VOLUME INCREASED ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MITRAL VALVE CALCIFICATION ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
NASAL SEPTUM DEVIATION ( 6 FDA reports)
NATURAL KILLER-CELL LYMPHOBLASTIC LYMPHOMA ( 6 FDA reports)
OBESITY ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
OSTEOLYSIS ( 6 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 6 FDA reports)
PANCREATIC PSEUDOCYST ( 6 FDA reports)
PAPILLOMA VIRAL INFECTION ( 6 FDA reports)
PARATHYROID TUMOUR BENIGN ( 6 FDA reports)
PCO2 DECREASED ( 6 FDA reports)
PEPTIC ULCER ( 6 FDA reports)
PERIANAL ABSCESS ( 6 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED STAGE IV ( 6 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
PLACENTAL DISORDER ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
POUCHITIS ( 6 FDA reports)
PROSTATE CANCER RECURRENT ( 6 FDA reports)
PROSTATOMEGALY ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PSEUDOPOLYP ( 6 FDA reports)
PSOAS ABSCESS ( 6 FDA reports)
PSORIATIC ARTHROPATHY ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
PULMONARY SEPSIS ( 6 FDA reports)
PYELOCALIECTASIS ( 6 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
RETINAL VEIN THROMBOSIS ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SEBACEOUS HYPERPLASIA ( 6 FDA reports)
SECONDARY AMYLOIDOSIS ( 6 FDA reports)
SINUSITIS BACTERIAL ( 6 FDA reports)
SKIN BURNING SENSATION ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SPINAL OPERATION ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
SPLENIC RUPTURE ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
STEATORRHOEA ( 6 FDA reports)
STREPTOCOCCAL SEPSIS ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 6 FDA reports)
TAKAYASU'S ARTERITIS ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
TONSILLAR HYPERTROPHY ( 6 FDA reports)
ABSCESS LIMB ( 5 FDA reports)
ACCIDENT ( 5 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 5 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 5 FDA reports)
ADENOVIRUS INFECTION ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ALVEOLOPLASTY ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANAL HAEMORRHAGE ( 5 FDA reports)
ANGER ( 5 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANOGENITAL WARTS ( 5 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 5 FDA reports)
ANTI-PLATELET ANTIBODY ( 5 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 5 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC VALVE DISEASE ( 5 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 5 FDA reports)
BACTERIAL DISEASE CARRIER ( 5 FDA reports)
BARRETT'S OESOPHAGUS ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BILIARY ANASTOMOSIS ( 5 FDA reports)
BLOOD BLISTER ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 5 FDA reports)
BODY TINEA ( 5 FDA reports)
BONE DEBRIDEMENT ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
BONE TUBERCULOSIS ( 5 FDA reports)
BRAIN NEOPLASM BENIGN ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHORIORETINITIS ( 5 FDA reports)
CHRONIC HEPATITIS ( 5 FDA reports)
COLORECTAL CANCER ( 5 FDA reports)
COLOSTOMY ( 5 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 5 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
CRYPTORCHISM ( 5 FDA reports)
CULTURE POSITIVE ( 5 FDA reports)
CYTOKINE STORM ( 5 FDA reports)
DEATH NEONATAL ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DENGUE FEVER ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DERMAL CYST ( 5 FDA reports)
DIABETIC COMPLICATION ( 5 FDA reports)
DIPLEGIA ( 5 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EYE ALLERGY ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
FIBROADENOMA OF BREAST ( 5 FDA reports)
FIBROUS HISTIOCYTOMA ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
GASTROENTERITIS NOROVIRUS ( 5 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 5 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GESTATIONAL HYPERTENSION ( 5 FDA reports)
GINGIVAL DISORDER ( 5 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE VIII ( 5 FDA reports)
GROIN ABSCESS ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HELLP SYNDROME ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATECTOMY ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HEPATITIS VIRAL ( 5 FDA reports)
HIDRADENITIS ( 5 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 5 FDA reports)
HYPOPYON ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
INCISION SITE COMPLICATION ( 5 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INJECTION SITE VESICLES ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
INTERVERTEBRAL DISCITIS ( 5 FDA reports)
INTESTINAL ANASTOMOSIS ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
INTESTINAL VILLI ATROPHY ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
KLEBSIELLA SEPSIS ( 5 FDA reports)
KLEBSIELLA TEST POSITIVE ( 5 FDA reports)
LEGIONELLA INFECTION ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LISTERIA SEPSIS ( 5 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 5 FDA reports)
LONG QT SYNDROME ( 5 FDA reports)
LOWER EXTREMITY MASS ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 5 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 5 FDA reports)
MENINGITIS HERPES ( 5 FDA reports)
METASTASES TO BONE MARROW ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MITRAL VALVE ATRESIA ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCLE INJURY ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
NEONATAL ANURIA ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
NIPPLE DISORDER ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OEDEMA MOUTH ( 5 FDA reports)
OEDEMA MUCOSAL ( 5 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
OLFACTORY NERVE DISORDER ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
OPHTHALMOPLEGIA ( 5 FDA reports)
OPTIC NERVE DISORDER ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
PERIPHERAL NERVE OPERATION ( 5 FDA reports)
PLACENTA PRAEVIA ( 5 FDA reports)
PLASMA CELL DISORDER ( 5 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 5 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROCTOCOLITIS ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 5 FDA reports)
PULMONARY CAVITATION ( 5 FDA reports)
PUPIL FIXED ( 5 FDA reports)
PURULENCE ( 5 FDA reports)
RECTAL CANCER METASTATIC ( 5 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL ISCHAEMIA ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 5 FDA reports)
RETICULOCYTE COUNT DECREASED ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 5 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SMALL INTESTINAL RESECTION ( 5 FDA reports)
SOFT TISSUE INFECTION ( 5 FDA reports)
SOMATOFORM DISORDER ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
SWEAT GLAND INFECTION ( 5 FDA reports)
TENSION ( 5 FDA reports)
THERAPEUTIC PROCEDURE ( 5 FDA reports)
THORACOTOMY ( 5 FDA reports)
THYMOMA ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TINEA VERSICOLOUR ( 5 FDA reports)
TONGUE ULCERATION ( 5 FDA reports)
TOOTH ABSCESS ( 5 FDA reports)
TOOTH DISORDER ( 5 FDA reports)
TOOTH LOSS ( 5 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TRACHEAL ULCER ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
VASCULAR OCCLUSION ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 5 FDA reports)
VERTEBROPLASTY ( 5 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 5 FDA reports)
VISCERAL LEISHMANIASIS ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
WEIGHT GAIN POOR ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
XXYY SYNDROME ( 5 FDA reports)
TOTAL BILE ACIDS INCREASED ( 4 FDA reports)
TRICHOSTASIS SPINULOSA ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
ULNA FRACTURE ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
URATE NEPHROPATHY ( 4 FDA reports)
URINARY BLADDER EXCISION ( 4 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 4 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 4 FDA reports)
VASCULAR CALCIFICATION ( 4 FDA reports)
VASCULITIC RASH ( 4 FDA reports)
VENOUS HAEMORRHAGE ( 4 FDA reports)
VESICOURETERIC REFLUX ( 4 FDA reports)
VIRAL MUTATION IDENTIFIED ( 4 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VITAMIN B12 DECREASED ( 4 FDA reports)
VITREOUS FLOATERS ( 4 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WHITE BLOOD CELL DISORDER ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL SEPSIS ( 4 FDA reports)
ABDOMINAL WALL DISORDER ( 4 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 4 FDA reports)
ABSCESS FUNGAL ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAEMIA NEONATAL ( 4 FDA reports)
ANAESTHESIA ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANORECTAL OPERATION ( 4 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AORTIC INJURY ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APLASIA CUTIS CONGENITA ( 4 FDA reports)
APPENDICECTOMY ( 4 FDA reports)
APTYALISM ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 4 FDA reports)
BENIGN NEOPLASM ( 4 FDA reports)
BEZOAR ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BLAST CELLS PRESENT ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLINDNESS TRANSIENT ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 4 FDA reports)
BLOOD CHOLESTEROL ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
BONE FRAGMENTATION ( 4 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BRADYCARDIA NEONATAL ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BREAST ADENOMA ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CALCULUS URINARY ( 4 FDA reports)
CATHETER PLACEMENT ( 4 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERVIX CARCINOMA STAGE II ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHLAMYDIAL INFECTION ( 4 FDA reports)
CHONDROLYSIS ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CHROMOSOME ABNORMALITY ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLON CANCER STAGE IV ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONGENITAL ANOMALY OF ADRENAL GLAND ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CORNEAL INFECTION ( 4 FDA reports)
COXSACKIE VIRAL INFECTION ( 4 FDA reports)
CRANIOCEREBRAL INJURY ( 4 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 4 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
DENTAL CLEANING ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE I ( 4 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ENDOPHTHALMITIS ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ENZYME ABNORMALITY ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOETAL MALPRESENTATION ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
FUNGUS CULTURE POSITIVE ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRAFT INFECTION ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
H1N1 INFLUENZA ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMOBILIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HAIR COLOUR CHANGES ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 4 FDA reports)
HERPES SEPSIS ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HIV TEST POSITIVE ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERPLASIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 4 FDA reports)
HYPOTONIA NEONATAL ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INHIBITORY DRUG INTERACTION ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE PAPULE ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 4 FDA reports)
INTESTINAL STOMA ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KERATITIS BACTERIAL ( 4 FDA reports)
KLEBSIELLA BACTERAEMIA ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
KNEE DEFORMITY ( 4 FDA reports)
LACTOSE INTOLERANCE ( 4 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 4 FDA reports)
LASER THERAPY ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 4 FDA reports)
LESION EXCISION ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIFE SUPPORT ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LOCKED-IN SYNDROME ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 4 FDA reports)
MANIA ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MASS EXCISION ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 4 FDA reports)
METASTASES TO PLEURA ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MORAXELLA INFECTION ( 4 FDA reports)
MOROSE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOPATHY STEROID ( 4 FDA reports)
NAIL-PATELLA SYNDROME ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 4 FDA reports)
NEONATAL HYPONATRAEMIA ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
OESOPHAGEAL PERFORATION ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
OVARIAN EPITHELIAL CANCER ( 4 FDA reports)
PARESIS CRANIAL NERVE ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PERIOSTITIS ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PHAEHYPHOMYCOSIS ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PHOTODERMATOSIS ( 4 FDA reports)
PHYSICAL DISABILITY ( 4 FDA reports)
PLASMACYTOSIS ( 4 FDA reports)
PNEUMATOSIS ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMONIA HERPES VIRAL ( 4 FDA reports)
POLYCYTHAEMIA VERA ( 4 FDA reports)
POROKERATOSIS ( 4 FDA reports)
POSTOPERATIVE ABSCESS ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PROLONGED LABOUR ( 4 FDA reports)
PSEUDOLYMPHOMA ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
PYURIA ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 4 FDA reports)
RENAL ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RENAL VEIN THROMBOSIS ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RESPIRATORY PARALYSIS ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETROGNATHIA ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
RHODOCOCCUS INFECTION ( 4 FDA reports)
SCLERODERMA RENAL CRISIS ( 4 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SEPTIC EMBOLUS ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 4 FDA reports)
SMOOTH MUSCLE CELL NEOPLASM ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPINAL COLUMN INJURY ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SYPHILIS ( 4 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TELANGIECTASIA ( 4 FDA reports)
TEMPERATURE INTOLERANCE ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
TESTICULAR PAIN ( 4 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
THYMOMA MALIGNANT ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TONSILLAR DISORDER ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ACUTE PHASE REACTION ( 3 FDA reports)
ADENOVIRAL HEPATITIS ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AIR EMBOLISM ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 3 FDA reports)
ALOPECIA EFFLUVIUM ( 3 FDA reports)
ALOPECIA TOTALIS ( 3 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 3 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
ANAL INFLAMMATION ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
ASTROCYTOMA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL PERICARDITIS ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BIOPSY KIDNEY ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLADDER NEOPLASM SURGERY ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLEPHAROPACHYNSIS ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BLOOD VISCOSITY INCREASED ( 3 FDA reports)
BONE MARROW NECROSIS ( 3 FDA reports)
BOVINE TUBERCULOSIS ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BREAST ABSCESS ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST CANCER STAGE II ( 3 FDA reports)
BREAST CELLULITIS ( 3 FDA reports)
BREAST DISCHARGE ( 3 FDA reports)
BREAST FEEDING ( 3 FDA reports)
BRONCHIAL FISTULA ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRONCHIAL ULCERATION ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 3 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 3 FDA reports)
BURSITIS INFECTIVE ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CAMPYLOBACTER INFECTION ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOPULMONARY BYPASS ( 3 FDA reports)
CAROTID ARTERY DISSECTION ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
CERULOPLASMIN INCREASED ( 3 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CHOREOATHETOSIS ( 3 FDA reports)
CHORIOAMNIONITIS ( 3 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 3 FDA reports)
CHROMOBLASTOMYCOSIS ( 3 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLD AGGLUTININS POSITIVE ( 3 FDA reports)
COLECTOMY PARTIAL ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
CONDYLOMA ACUMINATUM ( 3 FDA reports)
CONGENITAL MEGAURETER ( 3 FDA reports)
CONGENITAL TERATOMA ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CORNEAL NEOVASCULARISATION ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CRYOGLOBULINS PRESENT ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DERMATITIS DIAPER ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DISORDER OF ORBIT ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
ENCEPHALITIS BRAIN STEM ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
ENTEROCOLONIC FISTULA ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ERYTHROLEUKAEMIA ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRIC VARICES ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL SURGERY ( 3 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 3 FDA reports)
GENE MUTATION ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLIOMA ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRANULOCYTOSIS ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAND DEFORMITY ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 3 FDA reports)
HEPATIC ATROPHY ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATIC VEIN THROMBOSIS ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS C RNA POSITIVE ( 3 FDA reports)
HIGH GRADE B-CELL LYMPHOMA BURKITT-LIKE LYMPHOMA ( 3 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 3 FDA reports)
HODGKIN'S DISEASE STAGE III ( 3 FDA reports)
HUMAN ANTICHIMERIC ANTIBODY POSITIVE ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE I INFECTION ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL FISTULA INFECTION ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
INTRAOCULAR LENS IMPLANT ( 3 FDA reports)
INTRAUTERINE INFECTION ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KIDNEY MALFORMATION ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 3 FDA reports)
LARYNGEAL INFLAMMATION ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LUNG WEDGE RESECTION ( 3 FDA reports)
LUPUS ENCEPHALITIS ( 3 FDA reports)
LYMPH GLAND INFECTION ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MALACOPLAKIA VESICAE ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MEDIASTINUM NEOPLASM ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTASES TO HEART ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTASES TO THORAX ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MITOCHONDRIAL MYOPATHY ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYOCARDIAC ABSCESS ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPENIA NEONATAL ( 3 FDA reports)
NICOTINIC ACID DEFICIENCY ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
OOPHORECTOMY ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
PAIN THRESHOLD DECREASED ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PALLANAESTHESIA ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PARANASAL SINUS DISCOMFORT ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PELIOSIS HEPATIS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 3 FDA reports)
PEYRONIE'S DISEASE ( 3 FDA reports)
PHARYNGEAL INFLAMMATION ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYCHONDRITIS ( 3 FDA reports)
POOR SUCKING REFLEX ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 3 FDA reports)
PREGNANCY TEST NEGATIVE ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROLONGED EXPIRATION ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PURINE METABOLISM DISORDER ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
PYOGENIC GRANULOMA ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RECTAL LESION ( 3 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 3 FDA reports)
RECTOVAGINAL SEPTUM ABSCESS ( 3 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 3 FDA reports)
RENAL AMYLOIDOSIS ( 3 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 3 FDA reports)
RENAL CORTICAL NECROSIS ( 3 FDA reports)
RENAL HAEMORRHAGE ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESECTION OF RECTUM ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RHINITIS HYPERTROPHIC ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SARCOMA METASTATIC ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SEPTAL PANNICULITIS ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SKIN BACTERIAL INFECTION ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SOFT TISSUE NEOPLASM ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPASTIC PARAPLEGIA ( 3 FDA reports)
SPERM COUNT DECREASED ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SPINDLE CELL SARCOMA ( 3 FDA reports)
SPLEEN PALPABLE ( 3 FDA reports)
SPLENITIS ( 3 FDA reports)
SPONDYLOARTHROPATHY ( 3 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STERNOTOMY ( 3 FDA reports)
STITCH ABSCESS ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUTURE RELATED COMPLICATION ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYNOVECTOMY ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TENOSYNOVITIS STENOSANS ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA METASTATIC ( 3 FDA reports)
TROPICAL SPASTIC PARESIS ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UPPER MOTOR NEURONE LESION ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY CASTS PRESENT ( 3 FDA reports)
UTERINE NEOPLASM ( 3 FDA reports)
UTERINE RUPTURE ( 3 FDA reports)
VENA CAVA FILTER INSERTION ( 3 FDA reports)
VENTRICULAR ASYSTOLE ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
VIRAL TEST POSITIVE ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VITRECTOMY ( 3 FDA reports)
VITRITIS ( 3 FDA reports)
VULVAL CANCER STAGE 0 ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRANSFUSION MICROCHIMERISM ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRANSPLANT ABSCESS ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRANSVERSE PRESENTATION ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ULTRASONIC ANGIOGRAM ABNORMAL ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URETERAL SPASM ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC REPAIR ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINARY FISTULA ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UTERINE ATONY ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VACCINATION FAILURE ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VASCULAR NEOPLASM ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITELLO-INTESTINAL DUCT REMNANT ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VITREOUS OPACITIES ( 2 FDA reports)
VON WILLEBRAND'S DISEASE ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
XERODERMA ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACANTHAMOEBA INFECTION ( 2 FDA reports)
ACANTHOLYSIS ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALVEOLAR PROTEINOSIS ( 2 FDA reports)
AMNIOTIC CAVITY DISORDER ( 2 FDA reports)
ANAL INFECTION ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANORECTAL STENOSIS ( 2 FDA reports)
ANOVULATORY CYCLE ( 2 FDA reports)
ANTERIOR CHAMBER CELL ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 2 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APOPTOSIS ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARRHYTHMIA NEONATAL ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTHRITIS FUNGAL ( 2 FDA reports)
ASTROCYTOMA MALIGNANT ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
BACILLARY ANGIOMATOSIS ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 2 FDA reports)
BENCE JONES PROTEINURIA ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BILE DUCT NECROSIS ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BIOPSY LUNG ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 2 FDA reports)
BLOOD FOLATE ABNORMAL ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST NECROSIS ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BUCCAL CAVITY PAPILLOMA ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BURKITT'S LEUKAEMIA ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOMA IN SITU ( 2 FDA reports)
CARCINOMA IN SITU OF SKIN ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CD4/CD8 RATIO DECREASED ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL FUNGAL INFECTION ( 2 FDA reports)
CEREBRAL SARCOIDOSIS ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHEILITIS GRANULOMATOSA ( 2 FDA reports)
CHEST WALL ABSCESS ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHLOASMA ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLEDOCHOENTEROSTOMY ( 2 FDA reports)
CHOLEDOCHOLITHOTOMY ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHOROIDITIS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COCHLEA IMPLANT ( 2 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLICATION OF DELIVERY ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL CYST ( 2 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL GRAFT REJECTION ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CUTANEOUS LEISHMANIASIS ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS DUODENITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DWARFISM ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR CANAL STENOSIS ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR MALFORMATION ( 2 FDA reports)
EAR NEOPLASM MALIGNANT ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROPHORESIS ABNORMAL ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ENCEPHALITIS ALLERGIC ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
ENCEPHALITIS POST MEASLES ( 2 FDA reports)
ENDOCARDIAL FIBROSIS ( 2 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EWING'S SARCOMA ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID RETRACTION ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTRITIS FUNGAL ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 2 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE I ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HBV DNA INCREASED ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC VEIN STENOSIS ( 2 FDA reports)
HEPATITIS B DNA ASSAY ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HEPATOPULMONARY SYNDROME ( 2 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 2 FDA reports)
HEREDITARY HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HISTOLOGY ABNORMAL ( 2 FDA reports)
HODGKIN'S DISEASE STAGE II ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPEROXALURIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPHAEMA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEECTOMY ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTION REACTIVATION ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INFLUENZA B VIRUS TEST POSITIVE ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTRACARDIAC MASS ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER GRAFT LOSS ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUPUS HEPATITIS ( 2 FDA reports)
LYMPH NODE PALPABLE ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA RECURRENT ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MASTOID DISORDER ( 2 FDA reports)
MASTOIDECTOMY ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MELANOCYTIC HYPERPLASIA ( 2 FDA reports)
MENINGEAL NEOPLASM ( 2 FDA reports)
MENINGITIS FUNGAL ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
METASTASES TO ABDOMINAL WALL ( 2 FDA reports)
METASTASES TO SALIVARY GLAND ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MILK ALLERGY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITOCHONDRIAL ENCEPHALOMYOPATHY ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 2 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOPERICARDITIS ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NECK DEFORMITY ( 2 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 2 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 2 FDA reports)
NECROTISING RETINITIS ( 2 FDA reports)
NECROTISING ULCERATIVE PERIODONTITIS ( 2 FDA reports)
NEPHROURETERECTOMY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NICOTINAMIDE DECREASED ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NORMAL TENSION GLAUCOMA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ABNORMAL ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULOMOTOR STUDY ABNORMAL ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESTRADIOL DECREASED ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
OPTIC DISC HAEMORRHAGE ( 2 FDA reports)
OPTIC DISCS BLURRED ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OSTEOMYELITIS FUNGAL ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARACOCCIDIOIDES INFECTION ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC KIDNEY ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERICARDITIS INFECTIVE ( 2 FDA reports)
PERICARDITIS LUPUS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED RECURRENT ( 2 FDA reports)
PERIPORTAL SINUS DILATATION ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL CYST ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGITIS BACTERIAL ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLEURAL NEOPLASM ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMONIA LIPOID ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
PORTAL VEIN STENOSIS ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ARTERIOPATHY ( 2 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RADIOTHERAPY TO SKIN ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL CANCER RECURRENT ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL PAPILLARY NECROSIS ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL LASER COAGULATION ( 2 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SEMINOMA ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SINGLE UMBILICAL ARTERY ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN HYPOPLASIA ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SKULL MALFORMATION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMATIC DELUSION ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPERM ANALYSIS ABNORMAL ( 2 FDA reports)
SPERM COUNT ZERO ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 2 FDA reports)
STENT REMOVAL ( 2 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SYNOSTOSIS ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TESTICULAR ABSCESS ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYROID CANCER METASTATIC ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
THYROID GLAND ABSCESS ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION EARLY ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACNE INFANTILE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACRODERMATITIS ENTEROPATHICA ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBINISM ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES STAGE I ( 1 FDA reports)
ANASTOMOTIC FISTULA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANTERIOR CHAMBER FLARE ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTISYNTHETASE SYNDROME ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE COMPLICATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATYPICAL FIBROXANTHOMA ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA HIGH GRADE ( 1 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF CERVIX UTERI ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE OUTPUT ABNORMAL ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIARY SPHINCTEROTOMY ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER ADENOCARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NECROSIS ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER TUMOUR RESECTION ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM NORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PROINSULIN INCREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE SCAN NORMAL ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH ALCOHOL TEST ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRUDZINSKI'S SIGN ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CERVIX CARCINOMA STAGE III ( 1 FDA reports)
CERVIX NEOPLASM ( 1 FDA reports)
CHEMICAL CYSTITIS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLEDOCHAL CYST ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHONDROSARCOMA ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHOROIDAL HAEMORRHAGE ( 1 FDA reports)
CHROMOSOMAL DELETION ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM TEST ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLON DYSPLASIA ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HEARING DISORDER ( 1 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 1 FDA reports)
CONGENITAL INGUINAL HERNIA ( 1 FDA reports)
CONGENITAL JAW MALFORMATION ( 1 FDA reports)
CONGENITAL OSTEODYSTROPHY ( 1 FDA reports)
CONGENITAL PYELOCALIECTASIS ( 1 FDA reports)
CONGENITAL RENAL CYST ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONGENITAL THROMBOCYTE DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL ENDOTHELIITIS ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF PRESSURE DECREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS MYOCARDITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEGENERATION OF UTERINE FIBROID ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATOFIBROSARCOMA ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIARRHOEA NEONATAL ( 1 FDA reports)
DIFFUSE MESANGIAL SCLEROSIS ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUGLAS' POUCH MASS ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG CLEARANCE INCREASED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INFECTION BACTERIAL ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
EATON-LAMBERT SYNDROME ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECZEMA HERPETICUM ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALITIS MENINGOCOCCAL ( 1 FDA reports)
ENCEPHALOCELE ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
ENDOCARDIAL VARICES ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 1 FDA reports)
ENDOCARDITIS PSEUDOMONAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL CANCER RECURRENT ( 1 FDA reports)
ENDOMETRIOMA ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENTEROSTOMY CLOSURE ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDIDYMAL ENLARGEMENT ( 1 FDA reports)
EPIDIDYMECTOMY ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRA-OSSEOUS EWING'S SARCOMA RECURRENT ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECALURIA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FISTULA REPAIR ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUOROSIS ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOLLICULAR MUCINOSIS ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRUCTOSAMINE INCREASED ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRECTOMY PARTIAL ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS PSEUDOMONAS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GEOTRICHUM INFECTION ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE IV ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HBV-DNA POLYMERASE INCREASED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATICOJEJUNOSTOMY ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B E ANTIGEN ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOBLASTOMA ( 1 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTOPLASMOSIS CUTANEOUS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HLA MARKER STUDY POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE III ( 1 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 1 FDA reports)
HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTEROTOMY ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOGLOBULIN THERAPY ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED FISTULA ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE DRYNESS ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL T-CELL LYMPHOMA ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
JEJUNECTOMY ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DISLOCATION REDUCTION ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERNIG'S SIGN ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LARYNGOTRACHEITIS ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOERYTHROBLASTOSIS ( 1 FDA reports)
LEUKOPENIA NEONATAL ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LISTERIA ENCEPHALITIS ( 1 FDA reports)
LIVER INDURATION ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTOPENIA NEONATAL ( 1 FDA reports)
MACROSTOMIA ( 1 FDA reports)
MACULE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA METASTATIC ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT LYMPHOMA UNCLASSIFIABLE LOW GRADE ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 1 FDA reports)
MALIGNANT OVARIAN CYST ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MANDIBULOFACIAL DYSOSTOSIS ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM ILEUS ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL ABSCESS ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MEGALOBLASTS INCREASED ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS CANDIDA ( 1 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITOCHONDRIAL DNA DEPLETION ( 1 FDA reports)
MITOCHONDRIAL ENZYME DEFICIENCY ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOCUTANEOUS LEISHMANIASIS ( 1 FDA reports)
MUCOCUTANEOUS ULCERATION ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTI-VITAMIN DEFICIENCY ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE EPIPHYSEAL DYSPLASIA ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE GRAFT ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES RECURRENT ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDITIS MYCOTIC ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NECROTISING PANNICULITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE CONDUCTION STUDIES NORMAL ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NEUROCYSTICERCOSIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA METASTATIC ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NOCARDIA SEPSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NERVE NEOPLASM ( 1 FDA reports)
ORAL CAVITY NEOPLASM SURGERY ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGAN DONOR ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOSARCOMA LOCALISED ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE III ( 1 FDA reports)
OVARIAN GRANULOSA-THECA CELL TUMOUR ( 1 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 1 FDA reports)
OVARIAN LOW MALIGNANT POTENTIAL TUMOUR ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAGET'S DISEASE OF SKIN ( 1 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC ENZYMES ABNORMAL ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERINEAL FISTULA ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLETHYSMOGRAPHY ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POIKILODERMA ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMENORRHAGIA ( 1 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTOTOMY ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOMONONUCLEOSIS ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIOVENOUS FISTULA ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULMONARY VEIN STENOSIS ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL ENZYMES ABNORMAL ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CANCER STAGE I ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL GRANULAR CELL CARCINOMA ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL PELVIS FISTULA ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHITIS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT ULCERATION ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHESUS INCOMPATIBILITY ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SCAN WITH CONTRAST ABNORMAL ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC ARTHRITIS NEISSERIAL ( 1 FDA reports)
SEROCONVERSION TEST POSITIVE ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL MENINGIOMA BENIGN ( 1 FDA reports)
SPINAL VASCULAR DISORDER ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPOROTRICHOSIS ( 1 FDA reports)
SPUR CELL ANAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STARING ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STROKE VOLUME DECREASED ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SYNOVIORTHESIS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
T-CELL UNCLASSIFIABLE LYMPHOMA HIGH GRADE ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR GERM CELL CANCER METASTATIC ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBASTHENIA ( 1 FDA reports)
THYMUS ENLARGEMENT ( 1 FDA reports)
THYROID MALFORMATION ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR NEOPLASM ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC DILATATION OF COLON ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION WITH INCOMPATIBLE BLOOD ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TRUNCUS COELIACUS THROMBOSIS ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR RELATED COMPLICATION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPHUS ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URAEMIC GASTROPATHY ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETEROLYSIS PROCEDURE ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URINARY BLADDER SARCOMA ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ARSENIC DECREASED ( 1 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 1 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO DECREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOGRAM ABNORMAL ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VERTEBRAL ABSCESS ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VESICOURETERAL REFLUX SURGERY ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL HEPATITIS CARRIER ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITAMIN E DECREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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