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

PYREXIA ( 775 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 753 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 660 FDA reports)
VOMITING ( 593 FDA reports)
NAUSEA ( 583 FDA reports)
DIARRHOEA ( 533 FDA reports)
ANAEMIA ( 529 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 417 FDA reports)
DRUG INTERACTION ( 400 FDA reports)
DRUG INEFFECTIVE ( 312 FDA reports)
HYPERLIPIDAEMIA ( 309 FDA reports)
RENAL FAILURE ACUTE ( 309 FDA reports)
ABDOMINAL PAIN ( 303 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 298 FDA reports)
WEIGHT DECREASED ( 294 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 291 FDA reports)
DYSPNOEA ( 282 FDA reports)
RASH ( 279 FDA reports)
RENAL FAILURE ( 278 FDA reports)
HEADACHE ( 277 FDA reports)
LYMPHADENOPATHY ( 277 FDA reports)
DEATH ( 274 FDA reports)
JAUNDICE ( 261 FDA reports)
ASTHENIA ( 258 FDA reports)
MALAISE ( 255 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 254 FDA reports)
BLOOD BILIRUBIN INCREASED ( 253 FDA reports)
LIPODYSTROPHY ACQUIRED ( 247 FDA reports)
HEPATIC FAILURE ( 245 FDA reports)
PNEUMONIA ( 238 FDA reports)
LACTIC ACIDOSIS ( 235 FDA reports)
NEUTROPENIA ( 235 FDA reports)
SEPSIS ( 234 FDA reports)
HEPATITIS B ( 230 FDA reports)
DRUG RESISTANCE ( 229 FDA reports)
DIZZINESS ( 223 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 223 FDA reports)
COUGH ( 222 FDA reports)
FATIGUE ( 220 FDA reports)
CONFUSIONAL STATE ( 214 FDA reports)
RENAL IMPAIRMENT ( 213 FDA reports)
PREMATURE BABY ( 210 FDA reports)
HAEMOGLOBIN DECREASED ( 200 FDA reports)
PREGNANCY ( 198 FDA reports)
ASCITES ( 195 FDA reports)
HYPERTENSION ( 185 FDA reports)
DRUG TOXICITY ( 179 FDA reports)
LIVER DISORDER ( 175 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 174 FDA reports)
PANCYTOPENIA ( 173 FDA reports)
THROMBOCYTOPENIA ( 168 FDA reports)
HEPATIC CIRRHOSIS ( 166 FDA reports)
HIV INFECTION ( 166 FDA reports)
METABOLIC ACIDOSIS ( 160 FDA reports)
ABDOMINAL DISTENSION ( 159 FDA reports)
HEPATOTOXICITY ( 158 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 156 FDA reports)
ABORTION SPONTANEOUS ( 155 FDA reports)
CONDITION AGGRAVATED ( 155 FDA reports)
PAIN IN EXTREMITY ( 155 FDA reports)
HEPATITIS ( 151 FDA reports)
HEPATOMEGALY ( 148 FDA reports)
BLOOD CREATININE INCREASED ( 146 FDA reports)
CONVULSION ( 146 FDA reports)
DEHYDRATION ( 142 FDA reports)
OEDEMA PERIPHERAL ( 142 FDA reports)
MYALGIA ( 141 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 141 FDA reports)
PANCREATITIS ( 138 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 137 FDA reports)
MITOCHONDRIAL TOXICITY ( 136 FDA reports)
CACHEXIA ( 134 FDA reports)
BLOOD LACTIC ACID INCREASED ( 133 FDA reports)
ANOREXIA ( 132 FDA reports)
PORTAL HYPERTENSION ( 130 FDA reports)
KAPOSI'S SARCOMA ( 129 FDA reports)
HEPATIC ENCEPHALOPATHY ( 128 FDA reports)
TUBERCULOSIS ( 123 FDA reports)
NEUROPATHY PERIPHERAL ( 120 FDA reports)
DIABETES MELLITUS ( 119 FDA reports)
HYPOTENSION ( 117 FDA reports)
HYPERLACTACIDAEMIA ( 115 FDA reports)
PAIN ( 115 FDA reports)
MUSCULAR WEAKNESS ( 114 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 114 FDA reports)
LIPOATROPHY ( 111 FDA reports)
RESPIRATORY FAILURE ( 111 FDA reports)
TACHYCARDIA ( 111 FDA reports)
CHOLESTASIS ( 110 FDA reports)
DISEASE RECURRENCE ( 110 FDA reports)
HYPOKALAEMIA ( 110 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 109 FDA reports)
DEPRESSION ( 108 FDA reports)
OSTEONECROSIS ( 108 FDA reports)
PLATELET COUNT DECREASED ( 108 FDA reports)
STEVENS-JOHNSON SYNDROME ( 108 FDA reports)
AGITATION ( 107 FDA reports)
DECREASED APPETITE ( 107 FDA reports)
RHABDOMYOLYSIS ( 107 FDA reports)
VIRAL LOAD INCREASED ( 107 FDA reports)
HYPOAESTHESIA ( 105 FDA reports)
MULTI-ORGAN FAILURE ( 105 FDA reports)
ORAL CANDIDIASIS ( 105 FDA reports)
ARTHRALGIA ( 103 FDA reports)
CAESAREAN SECTION ( 102 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 102 FDA reports)
SPLENOMEGALY ( 100 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 97 FDA reports)
LEUKOPENIA ( 96 FDA reports)
BACK PAIN ( 94 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 94 FDA reports)
DYSPHAGIA ( 94 FDA reports)
ABDOMINAL PAIN UPPER ( 93 FDA reports)
EYELID PTOSIS ( 93 FDA reports)
HEPATIC ENZYME INCREASED ( 93 FDA reports)
ACUTE HEPATIC FAILURE ( 92 FDA reports)
VIRAL MUTATION IDENTIFIED ( 92 FDA reports)
HEPATITIS C ( 91 FDA reports)
STILLBIRTH ( 91 FDA reports)
MYOPATHY ( 90 FDA reports)
PROTEINURIA ( 89 FDA reports)
DIPLOPIA ( 87 FDA reports)
PRURITUS ( 87 FDA reports)
SEPTIC SHOCK ( 85 FDA reports)
GAIT DISTURBANCE ( 84 FDA reports)
ABORTION INDUCED ( 83 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 83 FDA reports)
NERVOUS SYSTEM DISORDER ( 83 FDA reports)
SOMNOLENCE ( 83 FDA reports)
GASTROENTERITIS ( 82 FDA reports)
HYPERSENSITIVITY ( 81 FDA reports)
INSOMNIA ( 81 FDA reports)
CARDIAC FAILURE ( 80 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 80 FDA reports)
VANISHING BILE DUCT SYNDROME ( 80 FDA reports)
CHEST PAIN ( 79 FDA reports)
GASTROINTESTINAL DISORDER ( 78 FDA reports)
HYPERGLYCAEMIA ( 78 FDA reports)
STAPHYLOCOCCAL INFECTION ( 78 FDA reports)
TRANSAMINASES INCREASED ( 78 FDA reports)
HEPATIC STEATOSIS ( 76 FDA reports)
HERPES ZOSTER ( 76 FDA reports)
HYPERBILIRUBINAEMIA ( 76 FDA reports)
PLEURAL EFFUSION ( 75 FDA reports)
BRADYCARDIA ( 73 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 73 FDA reports)
RESPIRATORY DISTRESS ( 73 FDA reports)
PHARYNGITIS ( 72 FDA reports)
TRANSPLANT REJECTION ( 72 FDA reports)
ERYTHEMA ( 71 FDA reports)
MYOCARDIAL INFARCTION ( 71 FDA reports)
RASH MACULO-PAPULAR ( 71 FDA reports)
CHILLS ( 70 FDA reports)
CONSTIPATION ( 70 FDA reports)
DEEP VEIN THROMBOSIS ( 70 FDA reports)
HEPATOSPLENOMEGALY ( 70 FDA reports)
VARICES OESOPHAGEAL ( 70 FDA reports)
HYPONATRAEMIA ( 69 FDA reports)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ( 69 FDA reports)
PALPITATIONS ( 67 FDA reports)
CARDIAC MURMUR ( 66 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 65 FDA reports)
WEIGHT INCREASED ( 65 FDA reports)
LYMPHOMA ( 64 FDA reports)
BLOOD AMYLASE INCREASED ( 63 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 63 FDA reports)
HEPATIC NECROSIS ( 63 FDA reports)
RENAL TUBULAR DISORDER ( 63 FDA reports)
FEBRILE NEUTROPENIA ( 62 FDA reports)
TREATMENT NONCOMPLIANCE ( 62 FDA reports)
BLOOD HIV RNA INCREASED ( 61 FDA reports)
CARDIOMYOPATHY ( 61 FDA reports)
DRUG HYPERSENSITIVITY ( 61 FDA reports)
GASTRITIS ( 61 FDA reports)
TACHYPNOEA ( 61 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 60 FDA reports)
ARRHYTHMIA ( 59 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 58 FDA reports)
LETHARGY ( 58 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 58 FDA reports)
NEPHROLITHIASIS ( 58 FDA reports)
PRODUCTIVE COUGH ( 58 FDA reports)
BLOOD PRESSURE DECREASED ( 57 FDA reports)
BLOOD URIC ACID INCREASED ( 57 FDA reports)
CALCULUS URINARY ( 57 FDA reports)
NEPHROTIC SYNDROME ( 57 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 55 FDA reports)
CUSHING'S SYNDROME ( 55 FDA reports)
INTRA-UTERINE DEATH ( 55 FDA reports)
LIVER TRANSPLANT ( 55 FDA reports)
GRAFT DYSFUNCTION ( 54 FDA reports)
PANCREATITIS ACUTE ( 54 FDA reports)
PARAESTHESIA ( 54 FDA reports)
PULMONARY EMBOLISM ( 54 FDA reports)
MELAENA ( 53 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 53 FDA reports)
OVERDOSE ( 53 FDA reports)
PULMONARY HYPERTENSION ( 53 FDA reports)
PULMONARY TUBERCULOSIS ( 53 FDA reports)
BLOOD GLUCOSE INCREASED ( 52 FDA reports)
HYPERKALAEMIA ( 52 FDA reports)
NEPHRITIS INTERSTITIAL ( 52 FDA reports)
RENAL DISORDER ( 52 FDA reports)
COAGULOPATHY ( 51 FDA reports)
HYPOPHOSPHATAEMIA ( 51 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 51 FDA reports)
SMALL FOR DATES BABY ( 51 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 50 FDA reports)
INFLUENZA LIKE ILLNESS ( 50 FDA reports)
PORTAL VEIN THROMBOSIS ( 50 FDA reports)
CARDIAC ARREST ( 49 FDA reports)
CONGENITAL ANOMALY ( 49 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 49 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 49 FDA reports)
ENCEPHALOPATHY ( 49 FDA reports)
GUILLAIN-BARRE SYNDROME ( 49 FDA reports)
HAEMATURIA ( 49 FDA reports)
OSTEOPOROSIS ( 49 FDA reports)
CHOLELITHIASIS ( 48 FDA reports)
DISEASE PROGRESSION ( 48 FDA reports)
FALL ( 48 FDA reports)
FANCONI SYNDROME ACQUIRED ( 48 FDA reports)
MENTAL STATUS CHANGES ( 48 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 47 FDA reports)
DYSARTHRIA ( 47 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 47 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 47 FDA reports)
INFECTION ( 47 FDA reports)
LIPASE INCREASED ( 47 FDA reports)
NEPHROPATHY TOXIC ( 47 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 47 FDA reports)
BLOOD SODIUM DECREASED ( 46 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 46 FDA reports)
FANCONI SYNDROME ( 46 FDA reports)
DISORIENTATION ( 45 FDA reports)
SYNCOPE ( 45 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 44 FDA reports)
SKIN LESION ( 44 FDA reports)
ANXIETY ( 43 FDA reports)
CRYPTOCOCCOSIS ( 43 FDA reports)
LYMPHADENITIS ( 43 FDA reports)
OCULAR ICTERUS ( 43 FDA reports)
OSTEOMALACIA ( 43 FDA reports)
DEPRESSED MOOD ( 42 FDA reports)
DRUG ERUPTION ( 42 FDA reports)
DRUG LEVEL INCREASED ( 42 FDA reports)
PALLOR ( 42 FDA reports)
AIDS ENCEPHALOPATHY ( 41 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 41 FDA reports)
BIOPSY LIVER ABNORMAL ( 41 FDA reports)
CARDIOMEGALY ( 41 FDA reports)
CEREBRAL HAEMORRHAGE ( 41 FDA reports)
CHOLANGITIS ( 41 FDA reports)
HAEMATEMESIS ( 41 FDA reports)
HYPOXIA ( 41 FDA reports)
MENTAL DISORDER ( 41 FDA reports)
PARKINSONISM ( 41 FDA reports)
URINARY TRACT INFECTION ( 41 FDA reports)
COMA ( 40 FDA reports)
CYTOLYTIC HEPATITIS ( 40 FDA reports)
HAEMATOCHEZIA ( 40 FDA reports)
HAEMOPTYSIS ( 40 FDA reports)
LOSS OF CONSCIOUSNESS ( 40 FDA reports)
NO THERAPEUTIC RESPONSE ( 40 FDA reports)
SCLERAL DISCOLOURATION ( 40 FDA reports)
THERAPY NON-RESPONDER ( 40 FDA reports)
VISION BLURRED ( 40 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 39 FDA reports)
CANDIDIASIS ( 39 FDA reports)
HAEMORRHAGE ( 39 FDA reports)
IRRITABILITY ( 39 FDA reports)
SUBDURAL HAEMATOMA ( 39 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 39 FDA reports)
HYPERCHOLESTEROLAEMIA ( 38 FDA reports)
HYPOTONIA ( 38 FDA reports)
TORSADE DE POINTES ( 38 FDA reports)
TREMOR ( 38 FDA reports)
ANAEMIA MACROCYTIC ( 37 FDA reports)
APHASIA ( 37 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 37 FDA reports)
HIV WASTING SYNDROME ( 37 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 37 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 37 FDA reports)
BLOOD POTASSIUM INCREASED ( 36 FDA reports)
GASTRIC ULCER ( 36 FDA reports)
HYPERURICAEMIA ( 36 FDA reports)
OEDEMA ( 36 FDA reports)
URTICARIA ( 36 FDA reports)
VIROLOGIC FAILURE ( 36 FDA reports)
BRAIN OEDEMA ( 35 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 35 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 35 FDA reports)
CHEST DISCOMFORT ( 35 FDA reports)
DELIRIUM ( 35 FDA reports)
DISTURBANCE IN ATTENTION ( 35 FDA reports)
PARALYSIS ( 35 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 35 FDA reports)
SWELLING FACE ( 35 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 35 FDA reports)
BLOOD PRESSURE INCREASED ( 34 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 34 FDA reports)
DRUG INTOLERANCE ( 34 FDA reports)
HEMIPARESIS ( 34 FDA reports)
HYPERTONIA ( 34 FDA reports)
MOVEMENT DISORDER ( 34 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 34 FDA reports)
RENAL TUBULAR NECROSIS ( 34 FDA reports)
URINE COLOUR ABNORMAL ( 34 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 33 FDA reports)
EPISTAXIS ( 33 FDA reports)
EROSIVE OESOPHAGITIS ( 33 FDA reports)
GRAND MAL CONVULSION ( 33 FDA reports)
LIVER TRANSPLANT REJECTION ( 33 FDA reports)
BLOOD ALBUMIN DECREASED ( 32 FDA reports)
BLOOD POTASSIUM DECREASED ( 32 FDA reports)
HEART RATE INCREASED ( 32 FDA reports)
HEPATIC FIBROSIS ( 32 FDA reports)
HEPATITIS FULMINANT ( 32 FDA reports)
HYPOALBUMINAEMIA ( 32 FDA reports)
HYPOSPADIAS ( 32 FDA reports)
BONE MARROW FAILURE ( 31 FDA reports)
COLITIS ( 31 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 31 FDA reports)
HALLUCINATION ( 31 FDA reports)
NEONATAL DISORDER ( 31 FDA reports)
NIGHTMARE ( 31 FDA reports)
RASH GENERALISED ( 31 FDA reports)
SPEECH DISORDER ( 31 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 31 FDA reports)
ABASIA ( 30 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 30 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 30 FDA reports)
NECROSIS ( 30 FDA reports)
OXYGEN SATURATION DECREASED ( 30 FDA reports)
RASH ERYTHEMATOUS ( 30 FDA reports)
TREATMENT FAILURE ( 30 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
VISUAL ACUITY REDUCED ( 30 FDA reports)
ACIDOSIS ( 29 FDA reports)
CONTUSION ( 29 FDA reports)
DIABETIC KETOACIDOSIS ( 29 FDA reports)
DRUG EFFECT DECREASED ( 29 FDA reports)
MITRAL VALVE INCOMPETENCE ( 29 FDA reports)
NEUTROPHIL COUNT DECREASED ( 29 FDA reports)
OPPORTUNISTIC INFECTION ( 29 FDA reports)
PNEUMOTHORAX ( 29 FDA reports)
PREMATURE LABOUR ( 29 FDA reports)
BACTERAEMIA ( 28 FDA reports)
BALANCE DISORDER ( 28 FDA reports)
BASEDOW'S DISEASE ( 28 FDA reports)
BONE PAIN ( 28 FDA reports)
DUODENAL ULCER ( 28 FDA reports)
HAEMATOCRIT DECREASED ( 28 FDA reports)
INFLAMMATION ( 28 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 28 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 28 FDA reports)
RENAL FAILURE CHRONIC ( 28 FDA reports)
UMBILICAL CORD ABNORMALITY ( 28 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 27 FDA reports)
AMNESIA ( 27 FDA reports)
APPENDICITIS ( 27 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 27 FDA reports)
DEVELOPMENTAL DELAY ( 27 FDA reports)
EPILEPSY ( 27 FDA reports)
HEPATITIS B DNA INCREASED ( 27 FDA reports)
MEMORY IMPAIRMENT ( 27 FDA reports)
MUSCLE HAEMORRHAGE ( 27 FDA reports)
NECK PAIN ( 27 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 27 FDA reports)
SINUSITIS ( 27 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 27 FDA reports)
TRISOMY 21 ( 27 FDA reports)
URINARY INCONTINENCE ( 27 FDA reports)
ALOPECIA ( 26 FDA reports)
BLOOD UREA INCREASED ( 26 FDA reports)
CHROMATURIA ( 26 FDA reports)
COORDINATION ABNORMAL ( 26 FDA reports)
DEATH NEONATAL ( 26 FDA reports)
FLATULENCE ( 26 FDA reports)
LEUKOENCEPHALOPATHY ( 26 FDA reports)
LUNG INFILTRATION ( 26 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 26 FDA reports)
OSTEOPENIA ( 26 FDA reports)
PRE-ECLAMPSIA ( 26 FDA reports)
PSYCHOTIC DISORDER ( 26 FDA reports)
RESPIRATORY RATE INCREASED ( 26 FDA reports)
SKIN ULCER ( 26 FDA reports)
VENTRICULAR TACHYCARDIA ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
VISUAL DISTURBANCE ( 26 FDA reports)
BACTERIAL INFECTION ( 25 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 25 FDA reports)
CHOLECYSTITIS ( 25 FDA reports)
CONJUNCTIVITIS ( 25 FDA reports)
CYANOSIS ( 25 FDA reports)
DYSLIPIDAEMIA ( 25 FDA reports)
ECTOPIC PREGNANCY ( 25 FDA reports)
GALLBLADDER DISORDER ( 25 FDA reports)
HYPOGLYCAEMIA ( 25 FDA reports)
IRON DEFICIENCY ANAEMIA ( 25 FDA reports)
MYCOBACTERIAL INFECTION ( 25 FDA reports)
SINUS TACHYCARDIA ( 25 FDA reports)
STOMATITIS ( 25 FDA reports)
ABSCESS ( 24 FDA reports)
BODY TEMPERATURE INCREASED ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
COAGULATION TIME PROLONGED ( 24 FDA reports)
ELECTROLYTE IMBALANCE ( 24 FDA reports)
ENCEPHALITIS ( 24 FDA reports)
GRANULOMA ( 24 FDA reports)
GYNAECOMASTIA ( 24 FDA reports)
HYPERTHERMIA ( 24 FDA reports)
LUNG DISORDER ( 24 FDA reports)
PATHOGEN RESISTANCE ( 24 FDA reports)
RASH MACULAR ( 24 FDA reports)
RESPIRATORY ARREST ( 24 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 23 FDA reports)
ATRIAL FIBRILLATION ( 23 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 23 FDA reports)
BRONCHOPNEUMONIA ( 23 FDA reports)
COGNITIVE DISORDER ( 23 FDA reports)
DRY MOUTH ( 23 FDA reports)
DYSKINESIA ( 23 FDA reports)
EXTRASYSTOLES ( 23 FDA reports)
FOETAL GROWTH RETARDATION ( 23 FDA reports)
HEPATITIS B VIRUS ( 23 FDA reports)
HUMAN IMMUNODEFICIENCY VIRUS TRANSMISSION ( 23 FDA reports)
MYOCARDITIS ( 23 FDA reports)
NORMAL NEWBORN ( 23 FDA reports)
POLYDACTYLY ( 23 FDA reports)
PROTHROMBIN TIME PROLONGED ( 23 FDA reports)
SUICIDE ATTEMPT ( 23 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 23 FDA reports)
VIRAL INFECTION ( 23 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 22 FDA reports)
AORTIC VALVE INCOMPETENCE ( 22 FDA reports)
CARDIO-RESPIRATORY ARREST ( 22 FDA reports)
CEREBELLAR SYNDROME ( 22 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 22 FDA reports)
EYE DISORDER ( 22 FDA reports)
GENERALISED OEDEMA ( 22 FDA reports)
HAEMOLYTIC ANAEMIA ( 22 FDA reports)
HYPERCALCAEMIA ( 22 FDA reports)
HYPERHIDROSIS ( 22 FDA reports)
MULTIPLE FRACTURES ( 22 FDA reports)
PULMONARY OEDEMA ( 22 FDA reports)
SEBORRHOEIC DERMATITIS ( 22 FDA reports)
SHOCK ( 22 FDA reports)
SKIN EXFOLIATION ( 22 FDA reports)
SLEEP DISORDER ( 22 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 22 FDA reports)
UVEITIS ( 22 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 22 FDA reports)
ACCIDENTAL OVERDOSE ( 21 FDA reports)
CARDIOGENIC SHOCK ( 21 FDA reports)
CATARACT ( 21 FDA reports)
CELLULITIS ( 21 FDA reports)
DYSPNOEA EXERTIONAL ( 21 FDA reports)
DYSURIA ( 21 FDA reports)
HAEMANGIOMA ( 21 FDA reports)
HAEMODIALYSIS ( 21 FDA reports)
HBV DNA INCREASED ( 21 FDA reports)
HEPATORENAL SYNDROME ( 21 FDA reports)
HIV TEST POSITIVE ( 21 FDA reports)
MEDICATION ERROR ( 21 FDA reports)
MUCOSAL INFLAMMATION ( 21 FDA reports)
MUSCLE SPASMS ( 21 FDA reports)
URINE OUTPUT DECREASED ( 21 FDA reports)
ACUTE RESPIRATORY FAILURE ( 20 FDA reports)
APLASIA PURE RED CELL ( 20 FDA reports)
BLISTER ( 20 FDA reports)
CRYPTORCHISM ( 20 FDA reports)
ENTEROCOLITIS ( 20 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 20 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 20 FDA reports)
HYPERTHYROIDISM ( 20 FDA reports)
HYPOREFLEXIA ( 20 FDA reports)
INCORRECT DOSE ADMINISTERED ( 20 FDA reports)
KLEBSIELLA INFECTION ( 20 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
PLACENTAL INFARCTION ( 20 FDA reports)
POLYNEUROPATHY ( 20 FDA reports)
PSORIASIS ( 20 FDA reports)
PULMONARY INFARCTION ( 20 FDA reports)
RASH PRURITIC ( 20 FDA reports)
RESTLESSNESS ( 20 FDA reports)
SICK SINUS SYNDROME ( 20 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 20 FDA reports)
SWELLING ( 20 FDA reports)
VASCULITIS ( 20 FDA reports)
ABNORMAL BEHAVIOUR ( 19 FDA reports)
EOSINOPHILIA ( 19 FDA reports)
HAEMATOMA ( 19 FDA reports)
HEMIPLEGIA ( 19 FDA reports)
LIVER INJURY ( 19 FDA reports)
MENINGITIS ( 19 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 19 FDA reports)
NECROTISING COLITIS ( 19 FDA reports)
OFF LABEL USE ( 19 FDA reports)
RALES ( 19 FDA reports)
RENAL INJURY ( 19 FDA reports)
SENSORY DISTURBANCE ( 19 FDA reports)
TEARFULNESS ( 19 FDA reports)
UROSEPSIS ( 19 FDA reports)
ABDOMINAL HERNIA ( 18 FDA reports)
ADRENAL INSUFFICIENCY ( 18 FDA reports)
ARTHRITIS ( 18 FDA reports)
ARTHRITIS BACTERIAL ( 18 FDA reports)
ASTHMA ( 18 FDA reports)
ATELECTASIS ( 18 FDA reports)
ATRIAL SEPTAL DEFECT ( 18 FDA reports)
BLOOD BICARBONATE DECREASED ( 18 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 18 FDA reports)
DIALYSIS ( 18 FDA reports)
DISSEMINATED TUBERCULOSIS ( 18 FDA reports)
DYSPEPSIA ( 18 FDA reports)
FAILURE TO THRIVE ( 18 FDA reports)
HEART SOUNDS ABNORMAL ( 18 FDA reports)
HEPATITIS CHOLESTATIC ( 18 FDA reports)
HODGKIN'S DISEASE ( 18 FDA reports)
HYPOTHERMIA ( 18 FDA reports)
ILEUS ( 18 FDA reports)
INCONTINENCE ( 18 FDA reports)
INTERSTITIAL LUNG DISEASE ( 18 FDA reports)
METABOLIC DISORDER ( 18 FDA reports)
MOUTH ULCERATION ( 18 FDA reports)
NEPHROPATHY ( 18 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 18 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 18 FDA reports)
VIRAEMIA ( 18 FDA reports)
AMENORRHOEA ( 17 FDA reports)
AREFLEXIA ( 17 FDA reports)
BRAIN HERNIATION ( 17 FDA reports)
BREAST MASS ( 17 FDA reports)
CEREBRAL INFARCTION ( 17 FDA reports)
FEELING HOT ( 17 FDA reports)
HEPATITIS VIRAL ( 17 FDA reports)
HERPES SIMPLEX ( 17 FDA reports)
HERPES VIRUS INFECTION ( 17 FDA reports)
INJECTION SITE REACTION ( 17 FDA reports)
LEUKOCYTOSIS ( 17 FDA reports)
MOBILITY DECREASED ( 17 FDA reports)
MUSCLE ATROPHY ( 17 FDA reports)
MYELODYSPLASTIC SYNDROME ( 17 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 17 FDA reports)
NEUROLOGICAL SYMPTOM ( 17 FDA reports)
NIGHT SWEATS ( 17 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 17 FDA reports)
PERITONITIS ( 17 FDA reports)
RASH PAPULAR ( 17 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 17 FDA reports)
RESPIRATORY TRACT INFECTION ( 17 FDA reports)
SHOCK HAEMORRHAGIC ( 17 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 17 FDA reports)
ABDOMINAL DISCOMFORT ( 16 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 16 FDA reports)
ANGIOEDEMA ( 16 FDA reports)
ASPERGILLOSIS ( 16 FDA reports)
BLINDNESS ( 16 FDA reports)
BRADYPHRENIA ( 16 FDA reports)
DANDY-WALKER SYNDROME ( 16 FDA reports)
DRUG LEVEL DECREASED ( 16 FDA reports)
ENCEPHALITIS VIRAL ( 16 FDA reports)
FACIAL WASTING ( 16 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 16 FDA reports)
GOITRE ( 16 FDA reports)
HALLUCINATION, AUDITORY ( 16 FDA reports)
HEPATIC ENZYME ABNORMAL ( 16 FDA reports)
HYDRONEPHROSIS ( 16 FDA reports)
JAUNDICE CHOLESTATIC ( 16 FDA reports)
LIPOHYPERTROPHY ( 16 FDA reports)
LYMPH NODE TUBERCULOSIS ( 16 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 16 FDA reports)
MANIA ( 16 FDA reports)
MASS ( 16 FDA reports)
OPHTHALMOPLEGIA ( 16 FDA reports)
PERICARDIAL EFFUSION ( 16 FDA reports)
PERIPHERAL ISCHAEMIA ( 16 FDA reports)
POST PROCEDURAL COMPLICATION ( 16 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 16 FDA reports)
RIB FRACTURE ( 16 FDA reports)
SPINAL COMPRESSION FRACTURE ( 16 FDA reports)
URINARY RETENTION ( 16 FDA reports)
ADVERSE EVENT ( 15 FDA reports)
AMINOACIDURIA ( 15 FDA reports)
APHTHOUS STOMATITIS ( 15 FDA reports)
ATAXIA ( 15 FDA reports)
BACTERIAL SEPSIS ( 15 FDA reports)
BLOOD GLUCOSE DECREASED ( 15 FDA reports)
BLOOD MAGNESIUM DECREASED ( 15 FDA reports)
BRONCHOSPASM ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
DEAFNESS UNILATERAL ( 15 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 15 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 15 FDA reports)
EROSIVE DUODENITIS ( 15 FDA reports)
EXOMPHALOS ( 15 FDA reports)
FACIAL PALSY ( 15 FDA reports)
FAT REDISTRIBUTION ( 15 FDA reports)
FOETAL DISORDER ( 15 FDA reports)
GAZE PALSY ( 15 FDA reports)
HAEMARTHROSIS ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 15 FDA reports)
HYDROCEPHALUS ( 15 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 15 FDA reports)
OPISTHOTONUS ( 15 FDA reports)
PERITONITIS BACTERIAL ( 15 FDA reports)
PNEUMONIA BACTERIAL ( 15 FDA reports)
PURPURA ( 15 FDA reports)
PYELONEPHRITIS ( 15 FDA reports)
QUADRIPARESIS ( 15 FDA reports)
RESPIRATORY DISORDER ( 15 FDA reports)
RETINAL DETACHMENT ( 15 FDA reports)
STRABISMUS ( 15 FDA reports)
TOXIC SKIN ERUPTION ( 15 FDA reports)
TUBERCULOID LEPROSY ( 15 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 15 FDA reports)
ANAEMIA NEONATAL ( 14 FDA reports)
ANGINA UNSTABLE ( 14 FDA reports)
ANURIA ( 14 FDA reports)
BLOOD CHLORIDE DECREASED ( 14 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
CITROBACTER INFECTION ( 14 FDA reports)
CORONARY ARTERY DISEASE ( 14 FDA reports)
CREPITATIONS ( 14 FDA reports)
DERMATITIS ALLERGIC ( 14 FDA reports)
DIFFICULTY IN WALKING ( 14 FDA reports)
DYSGEUSIA ( 14 FDA reports)
ENDOCARDITIS ( 14 FDA reports)
FAECAL INCONTINENCE ( 14 FDA reports)
FAT TISSUE INCREASED ( 14 FDA reports)
FEELING COLD ( 14 FDA reports)
HYPOKINESIA ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
INFLUENZA ( 14 FDA reports)
LABORATORY TEST ABNORMAL ( 14 FDA reports)
LIPIDS INCREASED ( 14 FDA reports)
LOCAL SWELLING ( 14 FDA reports)
LUNG NEOPLASM MALIGNANT ( 14 FDA reports)
METASTASES TO LIVER ( 14 FDA reports)
PERICARDITIS ( 14 FDA reports)
PHOTOPHOBIA ( 14 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 14 FDA reports)
SICKLE CELL ANAEMIA ( 14 FDA reports)
SINOATRIAL BLOCK ( 14 FDA reports)
SINUS BRADYCARDIA ( 14 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 14 FDA reports)
TONSILLITIS ( 14 FDA reports)
TYPE 2 DIABETES MELLITUS ( 14 FDA reports)
VAGINAL HAEMORRHAGE ( 14 FDA reports)
VERTIGO POSITIONAL ( 14 FDA reports)
VIRAL HEPATITIS CARRIER ( 14 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 14 FDA reports)
ABDOMINAL TENDERNESS ( 13 FDA reports)
ACUTE ABDOMEN ( 13 FDA reports)
AGGRESSION ( 13 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 13 FDA reports)
ANAL CANCER ( 13 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 13 FDA reports)
APRAXIA ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK ( 13 FDA reports)
BLOOD CALCIUM DECREASED ( 13 FDA reports)
BLOOD CREATINE INCREASED ( 13 FDA reports)
BONE MARROW TOXICITY ( 13 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 13 FDA reports)
CHOLECYSTITIS ACUTE ( 13 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 13 FDA reports)
DILATATION VENTRICULAR ( 13 FDA reports)
ERYSIPELAS ( 13 FDA reports)
FALLOT'S TETRALOGY ( 13 FDA reports)
HAEMODYNAMIC INSTABILITY ( 13 FDA reports)
HYPERREFLEXIA ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
HYPOTONIA NEONATAL ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
MYOSITIS ( 13 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
NEUROTOXICITY ( 13 FDA reports)
NYSTAGMUS ( 13 FDA reports)
PAROTID GLAND ENLARGEMENT ( 13 FDA reports)
RENAL TUBULAR ACIDOSIS ( 13 FDA reports)
RETROVIRAL INFECTION ( 13 FDA reports)
SKIN DISORDER ( 13 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
TALIPES ( 13 FDA reports)
TOXOPLASMOSIS ( 13 FDA reports)
VISCERAL LEISHMANIASIS ( 13 FDA reports)
VOLVULUS ( 13 FDA reports)
ACNE ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
APATHY ( 12 FDA reports)
ARRHYTHMIA NEONATAL ( 12 FDA reports)
ASEPTIC NECROSIS BONE ( 12 FDA reports)
BLOOD VISCOSITY INCREASED ( 12 FDA reports)
BRAIN STEM HAEMORRHAGE ( 12 FDA reports)
BRAIN STEM SYNDROME ( 12 FDA reports)
CEREBRAL ATROPHY ( 12 FDA reports)
CERVIX CARCINOMA ( 12 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 12 FDA reports)
DERMATITIS EXFOLIATIVE ( 12 FDA reports)
DRUG ABUSER ( 12 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 12 FDA reports)
DRY SKIN ( 12 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 12 FDA reports)
ESCHERICHIA INFECTION ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
FEAR ( 12 FDA reports)
FLUID RETENTION ( 12 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
GLAUCOMA ( 12 FDA reports)
GLYCOSURIA ( 12 FDA reports)
HEPATITIS TOXIC ( 12 FDA reports)
HYPOTHYROIDISM ( 12 FDA reports)
IMMUNODEFICIENCY ( 12 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
LIP EROSION ( 12 FDA reports)
MAJOR DEPRESSION ( 12 FDA reports)
MUCOSAL DISCOLOURATION ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 12 FDA reports)
OLIGURIA ( 12 FDA reports)
ORTHOPNOEA ( 12 FDA reports)
PANCREATITIS CHRONIC ( 12 FDA reports)
PERIPHERAL COLDNESS ( 12 FDA reports)
POLYURIA ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
SQUAMOUS CELL CARCINOMA ( 12 FDA reports)
SYPHILIS ( 12 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
TUMOUR LYSIS SYNDROME ( 12 FDA reports)
VENTRICULAR ARRHYTHMIA ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ABDOMINAL PAIN LOWER ( 11 FDA reports)
AFFECT LABILITY ( 11 FDA reports)
ARTERIOSCLEROSIS ( 11 FDA reports)
ASPHYXIA ( 11 FDA reports)
BILE DUCT OBSTRUCTION ( 11 FDA reports)
BLEEDING VARICOSE VEIN ( 11 FDA reports)
BLOOD CULTURE POSITIVE ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BOVINE TUBERCULOSIS ( 11 FDA reports)
BREAST CANCER ( 11 FDA reports)
CARDIAC MALPOSITION ( 11 FDA reports)
CATATONIA ( 11 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 11 FDA reports)
CHRONIC HEPATITIS ( 11 FDA reports)
CSF PROTEIN INCREASED ( 11 FDA reports)
DELUSION ( 11 FDA reports)
DERMATITIS BULLOUS ( 11 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 11 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 11 FDA reports)
DYSPHONIA ( 11 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
HYPOPROTEINAEMIA ( 11 FDA reports)
HYPOVOLAEMIC SHOCK ( 11 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
ILL-DEFINED DISORDER ( 11 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 11 FDA reports)
INJURY ( 11 FDA reports)
INSULIN RESISTANCE ( 11 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 11 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 11 FDA reports)
LYMPHOCYTOSIS ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 11 FDA reports)
MENINGITIS TUBERCULOUS ( 11 FDA reports)
METASTASES TO LUNG ( 11 FDA reports)
MICROCEPHALY ( 11 FDA reports)
MIGRAINE ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
MULTI-ORGAN DISORDER ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 11 FDA reports)
OESOPHAGEAL CARCINOMA ( 11 FDA reports)
OSTEOARTHRITIS ( 11 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 11 FDA reports)
PLATELET COUNT INCREASED ( 11 FDA reports)
PROTEIN URINE PRESENT ( 11 FDA reports)
PSOAS ABSCESS ( 11 FDA reports)
PULMONARY SARCOIDOSIS ( 11 FDA reports)
PULSE ABSENT ( 11 FDA reports)
PURULENT DISCHARGE ( 11 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 11 FDA reports)
SKIN REACTION ( 11 FDA reports)
UPPER MOTOR NEURONE LESION ( 11 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 10 FDA reports)
BONE DISORDER ( 10 FDA reports)
CERVICAL DYSPLASIA ( 10 FDA reports)
ECCHYMOSIS ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
ENTEROCOCCAL INFECTION ( 10 FDA reports)
ERECTILE DYSFUNCTION ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
GENE MUTATION ( 10 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 10 FDA reports)
GLUCOSE URINE PRESENT ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
HAEMORRHAGIC DIATHESIS ( 10 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 10 FDA reports)
LIVE BIRTH ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
MALARIA ( 10 FDA reports)
MARROW HYPERPLASIA ( 10 FDA reports)
NEONATAL HYPONATRAEMIA ( 10 FDA reports)
NEPHRITIS ( 10 FDA reports)
NEUROPATHY ( 10 FDA reports)
OPTIC NEURITIS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
OTITIS MEDIA ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
PLACENTAL TRANSFUSION SYNDROME ( 10 FDA reports)
PLAGIOCEPHALY ( 10 FDA reports)
PULMONARY CONGESTION ( 10 FDA reports)
PYELECTASIA ( 10 FDA reports)
RETINOBLASTOMA UNILATERAL ( 10 FDA reports)
RHINITIS ( 10 FDA reports)
SEROTONIN SYNDROME ( 10 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 10 FDA reports)
STRESS ( 10 FDA reports)
SUBILEUS ( 10 FDA reports)
SUPERINFECTION ( 10 FDA reports)
TRANSFUSION REACTION ( 10 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 10 FDA reports)
ADRENAL SUPPRESSION ( 9 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 9 FDA reports)
ASTERIXIS ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
BORDERLINE LEPROSY ( 9 FDA reports)
BRAIN DAMAGE ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
CARDIOPULMONARY FAILURE ( 9 FDA reports)
CD4 LYMPHOCYTES ( 9 FDA reports)
CENTRAL OBESITY ( 9 FDA reports)
CEREBRAL DISORDER ( 9 FDA reports)
CHORDEE ( 9 FDA reports)
COLITIS ULCERATIVE ( 9 FDA reports)
COLON OPERATION ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
CRYOGLOBULINAEMIA ( 9 FDA reports)
DEMYELINATION ( 9 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
ESCHERICHIA SEPSIS ( 9 FDA reports)
FAECES DISCOLOURED ( 9 FDA reports)
FOLLICULITIS ( 9 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 9 FDA reports)
HEPATITIS C VIRUS ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HOSPITALISATION ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
HYPERAMYLASAEMIA ( 9 FDA reports)
IMMUNOSUPPRESSION ( 9 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 9 FDA reports)
JOINT STIFFNESS ( 9 FDA reports)
KERATITIS ( 9 FDA reports)
KUSSMAUL RESPIRATION ( 9 FDA reports)
LACTASE DEFICIENCY ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LIVER ABSCESS ( 9 FDA reports)
MEASLES ( 9 FDA reports)
NERVOUSNESS ( 9 FDA reports)
NEURALGIA ( 9 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 9 FDA reports)
ORCHITIS ( 9 FDA reports)
PAIN IN JAW ( 9 FDA reports)
PARANOIA ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PERIARTHRITIS ( 9 FDA reports)
PERONEAL NERVE PALSY ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
PINEALOBLASTOMA ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
PROTEIN TOTAL DECREASED ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
REBOUND EFFECT ( 9 FDA reports)
RENAL COLIC ( 9 FDA reports)
RETINITIS ( 9 FDA reports)
SCHISTOSOMIASIS ( 9 FDA reports)
SKIN TOXICITY ( 9 FDA reports)
SOMNAMBULISM ( 9 FDA reports)
SPINAL FRACTURE ( 9 FDA reports)
SPLENIC RUPTURE ( 9 FDA reports)
STOMACH DISCOMFORT ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
STRONGYLOIDIASIS ( 9 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
UNEVALUABLE EVENT ( 9 FDA reports)
VENOUS THROMBOSIS ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
ACUTE PSYCHOSIS ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
AMYOTROPHY ( 8 FDA reports)
ANAEMIA MEGALOBLASTIC ( 8 FDA reports)
ANGIOPATHY ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 8 FDA reports)
BIOPSY BREAST ( 8 FDA reports)
BLADDER PAIN ( 8 FDA reports)
BLOOD CREATININE ABNORMAL ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
CALCULUS URETERIC ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
COMA HEPATIC ( 8 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 8 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 8 FDA reports)
DEFORMITY THORAX ( 8 FDA reports)
DIABETES INSIPIDUS ( 8 FDA reports)
DIAPHRAGMATIC APLASIA ( 8 FDA reports)
EAR PAIN ( 8 FDA reports)
EMOTIONAL DISORDER ( 8 FDA reports)
EUPHORIC MOOD ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
FAT ATROPHY ( 8 FDA reports)
FEBRILE CONVULSION ( 8 FDA reports)
GASTRIC DISORDER ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
GASTROINTESTINAL PERFORATION ( 8 FDA reports)
GIARDIASIS ( 8 FDA reports)
GINGIVAL BLEEDING ( 8 FDA reports)
GINGIVITIS ULCERATIVE ( 8 FDA reports)
HAEMATOTOXICITY ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 8 FDA reports)
HICCUPS ( 8 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 8 FDA reports)
HYPERCREATININAEMIA ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
ILEAL ULCER ( 8 FDA reports)
INGUINAL HERNIA ( 8 FDA reports)
INJECTION SITE ULCER ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LEFT VENTRICULAR FAILURE ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
LYMPHOEDEMA ( 8 FDA reports)
MENINGITIS ASEPTIC ( 8 FDA reports)
MENOPAUSAL SYMPTOMS ( 8 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 8 FDA reports)
METASTASES TO LYMPH NODES ( 8 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NEUTROPHILIA ( 8 FDA reports)
OESOPHAGITIS ( 8 FDA reports)
OLIGOHYDRAMNIOS ( 8 FDA reports)
PANCREATIC INSUFFICIENCY ( 8 FDA reports)
PAPILLOEDEMA ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PERSECUTORY DELUSION ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 8 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
PROTEIN TOTAL ABNORMAL ( 8 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
RHONCHI ( 8 FDA reports)
SALMONELLA SEPSIS ( 8 FDA reports)
SINUS ARREST ( 8 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 8 FDA reports)
TONGUE DISORDER ( 8 FDA reports)
ULCER ( 8 FDA reports)
UNRESPONSIVE TO STIMULI ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
WEIGHT GAIN POOR ( 8 FDA reports)
WOUND ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
XANTHELASMA ( 8 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 7 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
AIDS RELATED COMPLICATION ( 7 FDA reports)
ALCOHOL INTERACTION ( 7 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 7 FDA reports)
ANGIODYSPLASIA ( 7 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
ANION GAP DECREASED ( 7 FDA reports)
ANION GAP INCREASED ( 7 FDA reports)
ANOGENITAL WARTS ( 7 FDA reports)
AORTIC ANEURYSM RUPTURE ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
B-CELL LYMPHOMA ( 7 FDA reports)
BALLISMUS ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BEHCET'S SYNDROME ( 7 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 7 FDA reports)
BLOOD CALCIUM ABNORMAL ( 7 FDA reports)
BLOOD CALCIUM INCREASED ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 7 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD UREA ABNORMAL ( 7 FDA reports)
BONE DENSITY DECREASED ( 7 FDA reports)
BRAIN ABSCESS ( 7 FDA reports)
CONDYLOMA ACUMINATUM ( 7 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
EAR MALFORMATION ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 7 FDA reports)
FACTOR VIII INHIBITION ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
GALLOP RHYTHM PRESENT ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GASTRIC VARICES ( 7 FDA reports)
GASTROSCHISIS ( 7 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HEPATIC DISPLACEMENT ( 7 FDA reports)
HEPATITIS A ( 7 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 7 FDA reports)
HEPATOJUGULAR REFLUX ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPOCHOLESTEROLAEMIA ( 7 FDA reports)
HYPOURICAEMIA ( 7 FDA reports)
HYPOVENTILATION ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
IMPAIRED HEALING ( 7 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 7 FDA reports)
LIPOMATOSIS ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MEAN CELL VOLUME INCREASED ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
MULTIPLE MYELOMA ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 7 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
NEONATAL RESPIRATORY ARREST ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
PERITONEAL HAEMORRHAGE ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PLACENTAL DISORDER ( 7 FDA reports)
PNEUMATOSIS ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PNEUMONIA LEGIONELLA ( 7 FDA reports)
PNEUMOPERITONEUM ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
PSEUDOMONAL SEPSIS ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
PUPILS UNEQUAL ( 7 FDA reports)
RADIUS FRACTURE ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SKULL MALFORMATION ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
SYNOVITIS ( 7 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 7 FDA reports)
TUMOUR HAEMORRHAGE ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 7 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 7 FDA reports)
URINARY SEDIMENT ABNORMAL ( 7 FDA reports)
VACCINATION FAILURE ( 7 FDA reports)
VASCULITIS NECROTISING ( 7 FDA reports)
VASODILATATION ( 7 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ACID FAST BACILLI INFECTION ( 6 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
AMOEBIASIS ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
AORTIC VALVE DISEASE ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 6 FDA reports)
BLOOD URIC ACID DECREASED ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BURKITT'S LYMPHOMA ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CELL DEATH ( 6 FDA reports)
CEREBELLAR ATROPHY ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 6 FDA reports)
CHORIOAMNIONITIS ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
CONGENITAL CLAVICULAR AGENESIS ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
CSF PRESSURE INCREASED ( 6 FDA reports)
CSF TEST ABNORMAL ( 6 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
DERMATITIS ( 6 FDA reports)
DILATATION ATRIAL ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DRUG PRESCRIBING ERROR ( 6 FDA reports)
DYSPRAXIA ( 6 FDA reports)
EAR DISCOMFORT ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
EPIDIDYMITIS ( 6 FDA reports)
ERYTHEMA INFECTIOSUM ( 6 FDA reports)
EXANTHEM ( 6 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
FIBROSIS ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
FOETOR HEPATICUS ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GESTATIONAL DIABETES ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 6 FDA reports)
HYPERTROPHY ( 6 FDA reports)
INCREASED APPETITE ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
JC VIRUS INFECTION ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
KAPOSI'S SARCOMA AIDS RELATED ( 6 FDA reports)
LACTATE PYRUVATE RATIO INCREASED ( 6 FDA reports)
LICHENOID KERATOSIS ( 6 FDA reports)
LIMB MALFORMATION ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MICROCYTIC ANAEMIA ( 6 FDA reports)
MICROSPORIDIA INFECTION ( 6 FDA reports)
MONOPARESIS ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 6 FDA reports)
NEURODEGENERATIVE DISORDER ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
OPTIC NERVE NEOPLASM ( 6 FDA reports)
ORAL DISCOMFORT ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
ORAL LICHEN PLANUS ( 6 FDA reports)
PAPILLOMA ( 6 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PAROTID GLAND INFLAMMATION ( 6 FDA reports)
PERIANAL ABSCESS ( 6 FDA reports)
PERIORBITAL OEDEMA ( 6 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PROTHROMBIN TIME SHORTENED ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PYELOCALIECTASIS ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
REFLEXES ABNORMAL ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
SCAR ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SEMINOMA ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SPLENIC ABSCESS ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
SPLENIC LESION ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SUDDEN HEARING LOSS ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
THIRST ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
TONGUE BITING ( 6 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 6 FDA reports)
TRIGEMINAL NEURALGIA ( 6 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
VITRITIS ( 6 FDA reports)
VOCAL CORD POLYP ( 6 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
ACUTE HIV INFECTION ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
ASTROCYTOMA ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
AUTOIMMUNE THYROIDITIS ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 5 FDA reports)
BIOPSY BILE DUCT ABNORMAL ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD KETONE BODY INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BREAST ABSCESS ( 5 FDA reports)
BRONCHIOLITIS ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
CLEFT LIP ( 5 FDA reports)
COARCTATION OF THE AORTA ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
CONGENITAL HEPATOBILIARY ANOMALY ( 5 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 5 FDA reports)
CRYSTAL NEPHROPATHY ( 5 FDA reports)
CUBITAL TUNNEL SYNDROME ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
CUTANEOUS LEISHMANIASIS ( 5 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 5 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 5 FDA reports)
ERGOT POISONING ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
EXERCISE TOLERANCE DECREASED ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
EYE PRURITUS ( 5 FDA reports)
FIBULA FRACTURE ( 5 FDA reports)
FOETAL DISTRESS SYNDROME ( 5 FDA reports)
FOLATE DEFICIENCY ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTROINTESTINAL TOXICITY ( 5 FDA reports)
GINGIVAL INFECTION ( 5 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 5 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
GRANULOCYTOPENIA ( 5 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 5 FDA reports)
HAEMANGIOMA CONGENITAL ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HEPATIC INFECTION ( 5 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 5 FDA reports)
HYDROCELE ( 5 FDA reports)
HYDROPS FOETALIS ( 5 FDA reports)
HYPERAMMONAEMIA ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
HYPERSPLENISM ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
HYPOGONADISM ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOMANIA ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
ISOSPORIASIS ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
KWASHIORKOR ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LYMPHOCYTIC INFILTRATION ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MENTAL RETARDATION ( 5 FDA reports)
MITOCHONDRIAL DNA DELETION ( 5 FDA reports)
MITOCHONDRIAL DNA DEPLETION ( 5 FDA reports)
MITOCHONDRIAL MYOPATHY ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MUCOCUTANEOUS RASH ( 5 FDA reports)
MUSCLE ABSCESS ( 5 FDA reports)
NEOPLASM OF APPENDIX ( 5 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 5 FDA reports)
NEUROSYPHILIS ( 5 FDA reports)
NEUTROPENIA NEONATAL ( 5 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NODULE ( 5 FDA reports)
NOSE DEFORMITY ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PARESIS ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PLACENTA PRAEVIA ( 5 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
PROSTATIC ABSCESS ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 5 FDA reports)
PSEUDOMYXOMA PERITONEI ( 5 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 5 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RETICULOCYTE COUNT DECREASED ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TENDERNESS ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 5 FDA reports)
UNINTENDED PREGNANCY ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
URINE CALCIUM INCREASED ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VIRAL LOAD DECREASED ( 5 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
ADRENAL INSUFFICIENCY NEONATAL ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
AMOEBIC DYSENTERY ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAL ATRESIA ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 4 FDA reports)
ANGIOLIPOMA ( 4 FDA reports)
ANORECTAL DISORDER ( 4 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BLADDER NECK OBSTRUCTION ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CEPHALHAEMATOMA ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL ATROPHY CONGENITAL ( 4 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLITIS EROSIVE ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
CONGENITAL ABDOMINAL HERNIA ( 4 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
CONGENITAL DIAPHRAGMATIC ANOMALY ( 4 FDA reports)
CONGENITAL EYE DISORDER ( 4 FDA reports)
CONGENITAL FOOT MALFORMATION ( 4 FDA reports)
CONGENITAL HAND MALFORMATION ( 4 FDA reports)
CONGENITAL TOXOPLASMOSIS ( 4 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
CRANIAL NERVE DISORDER ( 4 FDA reports)
CREATININE URINE DECREASED ( 4 FDA reports)
CRYING ( 4 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
EJECTION FRACTION ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ENCOPRESIS ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FINE MOTOR DELAY ( 4 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
FRACTURED ISCHIUM ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTRITIS ATROPHIC ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HAEMORRHAGIC ASCITES ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 4 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 4 FDA reports)
HEPATITIS D ( 4 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 4 FDA reports)
HIP DYSPLASIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 4 FDA reports)
HYPOCAPNIA ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
ILEAL ATRESIA ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
KETONURIA ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LARYNGEAL ERYTHEMA ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LEISHMANIASIS ( 4 FDA reports)
LEPROSY ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LEUKOCYTURIA ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LOW SET EARS ( 4 FDA reports)
LOWER LIMB DEFORMITY ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
MECONIUM STAIN ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MICROANGIOPATHY ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MONOCYTOSIS ( 4 FDA reports)
MONONEUROPATHY ( 4 FDA reports)
MOTOR NEURONE DISEASE ( 4 FDA reports)
MOYAMOYA DISEASE ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
MYALGIA INTERCOSTAL ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NEOPLASM RECURRENCE ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 4 FDA reports)
PENILE SIZE REDUCED ( 4 FDA reports)
PERICARDIAL DISEASE ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PLEOCYTOSIS ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
PORENCEPHALY ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PREGNANCY OF PARTNER ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PROTEIN S DEFICIENCY ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RENAL GLYCOSURIA ( 4 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SALIVARY GLAND CALCULUS ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 4 FDA reports)
SEX HORMONE BINDING GLOBULIN DECREASED ( 4 FDA reports)
SHOULDER PAIN ( 4 FDA reports)
SKELETON DYSPLASIA ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
TERATOMA ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TUMOUR FLARE ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
UREA URINE DECREASED ( 4 FDA reports)
URETERIC DILATATION ( 4 FDA reports)
URINE PHOSPHATE DECREASED ( 4 FDA reports)
URINE PHOSPHORUS DECREASED ( 4 FDA reports)
URINE URIC ACID DECREASED ( 4 FDA reports)
URINE URIC ACID INCREASED ( 4 FDA reports)
URTICARIA CHRONIC ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABORTION THREATENED ( 3 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
AMNIOTIC CAVITY DISORDER ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APLASIA CUTIS CONGENITA ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPLICATION SITE NODULE ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ASPERGILLOMA ( 3 FDA reports)
ASPIRATION BIOPSY ( 3 FDA reports)
ASTROCYTOMA, LOW GRADE ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BILIARY TRACT INFECTION ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD KETONE BODY PRESENT ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD ZINC DECREASED ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BONE TUBERCULOSIS ( 3 FDA reports)
BRACHIAL PLEXUS INJURY ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRADYCARDIA FOETAL ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 3 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 3 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CEREBRAL MALARIA ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHOLANGITIS CHRONIC ( 3 FDA reports)
CHORIORETINITIS ( 3 FDA reports)
CLUBBING ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
COLORECTAL CANCER STAGE IV ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CONGENITAL CYSTIC LUNG ( 3 FDA reports)
CONGENITAL HIV INFECTION ( 3 FDA reports)
CONGENITAL NAEVUS ( 3 FDA reports)
CONGENITAL NYSTAGMUS ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CSF GLUCOSE ABNORMAL ( 3 FDA reports)
CYST RUPTURE ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DISORDER OF GLOBE ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSHIDROSIS ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ECLAMPSIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
ERB'S PALSY ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 3 FDA reports)
EXPOSURE VIA SEMEN ( 3 FDA reports)
EYES SUNKEN ( 3 FDA reports)
FACTOR VIII DEFICIENCY ( 3 FDA reports)
FALLOPIAN TUBE OBSTRUCTION ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOETAL MALFORMATION ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GENERAL NUTRITION DISORDER ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GENOTYPE DRUG RESISTANCE TEST ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HAIRY CELL LEUKAEMIA ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS C RNA POSITIVE ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HIV ASSOCIATED NEPHROPATHY ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCALCIURIA ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERTENSIVE HYDROCEPHALUS ( 3 FDA reports)
HYPERTROPHY BREAST ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
IRIDOCELE ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRITIS ( 3 FDA reports)
JOINT ARTHROPLASTY ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIVER CARCINOMA RUPTURED ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 3 FDA reports)
MENINGITIS COCCIDIOIDES ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MENINGORADICULITIS ( 3 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
MICROGNATHIA ( 3 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 3 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NECROTISING HERPETIC RETINOPATHY ( 3 FDA reports)
NECROTISING RETINITIS ( 3 FDA reports)
NEMATODIASIS ( 3 FDA reports)
NEONATAL INFECTION ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEURITIS ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
OROPHARYNGITIS FUNGAL ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PALLANAESTHESIA ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PENICILLIOSIS ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERITONEAL FIBROSIS ( 3 FDA reports)
PERITONEAL INFECTION ( 3 FDA reports)
PIERRE ROBIN SYNDROME ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PILONIDAL CYST CONGENITAL ( 3 FDA reports)
PLATELET TOXICITY ( 3 FDA reports)
PLEURAL ADHESION ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYP ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSYCHOMOTOR AGITATION ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL CYST HAEMORRHAGE ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RETINOBLASTOMA ( 3 FDA reports)
RETROGNATHIA ( 3 FDA reports)
RHODOCOCCUS INFECTION ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
RUBELLA ( 3 FDA reports)
SCROTAL DISORDER ( 3 FDA reports)
SELECTIVE ABORTION ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN OEDEMA ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SPASTIC PARAPLEGIA ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SPUTUM TEST ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
TESTIS CANCER ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TINEA CAPITIS ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE BILIRUBIN INCREASED ( 3 FDA reports)
URINE PHOSPHATE INCREASED ( 3 FDA reports)
URINE PHOSPHORUS INCREASED ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 3 FDA reports)
VAGINAL DISCHARGE ( 3 FDA reports)
VAGINAL LESION ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VIRAL RASH ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VITREOUS OPACITIES ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ZINC DEFICIENCY ( 3 FDA reports)
ABDOMINAL WALL ANOMALY ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED MACROCEPHALY ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ADENOVIRAL HEPATITIS ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL FISTULA INFECTION ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTISM ( 2 FDA reports)
BARTHOLIN'S CYST ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILIARY ANASTOMOSIS ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 2 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY DYSMORPHIC DISORDER ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE GIANT CELL TUMOUR BENIGN ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BULBAR PALSY ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
BUSCHKE-LOWENSTEIN'S TUMOUR ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CAPUT MEDUSAE ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVIX OPERATION ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHORIORETINAL SCAR ( 2 FDA reports)
CHROMOSOMAL MUTATION ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CHYLOTHORAX ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COMBINED IMMUNODEFICIENCY ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL BOWING OF LONG BONES ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 2 FDA reports)
CONGENITAL INGUINAL HERNIA ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGENITAL NOSE MALFORMATION ( 2 FDA reports)
CONGENITAL ORAL MALFORMATION ( 2 FDA reports)
CONGENITAL PYELOCALIECTASIS ( 2 FDA reports)
CONGENITAL SYPHILIS ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COXSACKIE VIRAL INFECTION ( 2 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 2 FDA reports)
CSF CULTURE POSITIVE ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CUPULOLITHIASIS ( 2 FDA reports)
CUTANEOUS SARCOIDOSIS ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTIC LYMPHANGIOMA ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DERMATITIS DIAPER ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTERITIS NECROTICANS ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
FACIAL NEURALGIA ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FIBROSARCOMA ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTRIC VOLVULUS ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC AMOEBIASIS ( 2 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS B POSITIVE ( 2 FDA reports)
HEPATITIS C RNA NEGATIVE ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATITIS E ANTIGEN POSITIVE ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HIGH ARCHED PALATE ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HISTIOCYTOSIS ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HUMAN ANTI-MOUSE ANTIBODY POSITIVE ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERPHOSPHATASAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOPHONESIS ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOTONY OF EYE ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFANTILE SPITTING UP ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INJECTION SITE EROSION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
ISCHAEMIC LIMB PAIN ( 2 FDA reports)
IVTH NERVE PARALYSIS ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LATENT AUTOIMMUNE DIABETES IN ADULTS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHATIC OBSTRUCTION ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MEDICAL OBSERVATION ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MICROGLOSSIA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUTAGENIC EFFECT ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NAIL PIGMENTATION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OTITIS MEDIA BACTERIAL ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARASITE DNA TEST POSITIVE ( 2 FDA reports)
PARASITE STOOL TEST POSITIVE ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC INFECTION ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERICARDIAL RUB ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PITUITARY CYST ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PREMATURE CLOSURE OF CRANIAL SUTURES ( 2 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PURULENT PERICARDITIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RADIATION MYELOPATHY ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RETROVIRAL REBOUND SYNDROME ( 2 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCAPHOCEPHALY ( 2 FDA reports)
SCLERAL HYPERAEMIA ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPLENIC EMBOLISM ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPOROTRICHOSIS ( 2 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBACUTE COMBINED CORD DEGENERATION ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SYMBLEPHARON ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THALASSAEMIA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYROID GLAND ABSCESS ( 2 FDA reports)
THYROIDITIS ACUTE ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXIC DILATATION OF COLON ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TRISOMY 18 ( 2 FDA reports)
TUBERCULID ( 2 FDA reports)
TUMOUR RUPTURE ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL DYSPLASIA ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VARICOPHLEBITIS ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 2 FDA reports)
VESICOURETERIC REFLUX ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL PRODUCT OF CONCEPTION ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 1 FDA reports)
ACQUIRED GENE MUTATION ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADACTYLY ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENALITIS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AIDS DEMENTIA COMPLEX ( 1 FDA reports)
AIDS RELATED COMPLEX ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBINISM ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID ABNORMAL ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNIOCENTESIS ABNORMAL ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANION GAP NORMAL ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL DIARRHOEA ( 1 FDA reports)
BACTERIAL DNA TEST POSITIVE ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY ISCHAEMIA ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLAST CELLS ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD HIV RNA ( 1 FDA reports)
BLOOD HIV RNA DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CARNITINE INCREASED ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CATARACT CONGENITAL ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEILITIS GRANULOMATOSA ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLD AGGLUTININS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL ARTERIOVENOUS FISTULA ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 1 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
CONGENITAL TERATOMA ( 1 FDA reports)
CONGENITAL TRACHEOMALACIA ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
COXSACKIE VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
CRANIOFACIAL DYSOSTOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF LACTATE INCREASED ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CUTANEOUS TUBERCULOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION IN NEWBORN ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DIVERTICULITIS OESOPHAGEAL ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL ATRESIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EBSTEIN'S ANOMALY ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EUTHANASIA ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE INFECTION SYPHILITIC ( 1 FDA reports)
EYE INFECTION TOXOPLASMAL ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACTOR II MUTATION ( 1 FDA reports)
FACTOR IX DEFICIENCY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FITZ-HUGH-CURTIS SYNDROME ( 1 FDA reports)
FLOPPY INFANT ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FREE FATTY ACIDS INCREASED ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS CSF TEST POSITIVE ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC HYPERPLASIA ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GENOTYPE DRUG RESISTANCE TEST ABNORMAL ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROUP B STREPTOCOCCUS NEONATAL SEPSIS ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOSALPINX ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B DNA ASSAY ( 1 FDA reports)
HEPATITIS C RNA ( 1 FDA reports)
HEPATITIS CHRONIC PERSISTENT ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HERBAL TOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HIV ANTIBODY POSITIVE ( 1 FDA reports)
HIV DISEASE PROGRESSION ( 1 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE DEPLETION TYPE STAGE IV ( 1 FDA reports)
HOLMES TREMOR ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOSTHENURIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMINENT ABORTION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNODEFICIENCY CONGENITAL ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION REACTIVATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFECTIVE ANEURYSM ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ATRESIA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
KERNIG'S SIGN ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS NON-ALCOHOLIC ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LACTATE PYRUVATE RATIO ABNORMAL ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEPROMATOUS LEPROSY ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIVER GRAFT LOSS ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO MUSCLE ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MINIMUM INHIBITORY CONCENTRATION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYCOBACTERIA URINE TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST NEGATIVE ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTIC PRESERVATION INJURY OF GRAFT ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 1 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
OBSTETRIC PROCEDURE COMPLICATION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARACOCCIDIOIDES INFECTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PARTIAL LIPODYSTROPHY ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PAST-POINTING ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOBIA OF FLYING ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POPLITEAL PULSE ABNORMAL ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST ABORTION HAEMORRHAGE ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY CEREBELLAR DEGENERATION ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PROGRESSIVE CEREBELLAR DEGENERATION ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDODIVERTICULAR DISEASE ( 1 FDA reports)
PSYCHIATRIC INVESTIGATION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY PERCUSSION TEST ABNORMALITY ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL ATRESIA ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL HYDROCELE ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SALIVARY GLAND CYST ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMOOTH MUSCLE CELL NEOPLASM ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYPHILIS GENITAL ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR INFARCTION ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROID TUBERCULOSIS ( 1 FDA reports)
THYROTOXIC PERIODIC PARALYSIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIGEMINAL PALSY ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULOMA OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TUBERCULOSIS OF EYE ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETERIC RUPTURE ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE AMINO ACID LEVEL INCREASED ( 1 FDA reports)
URINE CALCIUM DECREASED ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE URIC ACID ABNORMAL ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE INVERSION ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR CISTERNOSTOMY ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WATER POLLUTION ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)