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

PYREXIA ( 595 FDA reports)
DYSPNOEA ( 515 FDA reports)
FALL ( 395 FDA reports)
PAIN ( 382 FDA reports)
ANAEMIA ( 373 FDA reports)
VOMITING ( 372 FDA reports)
NAUSEA ( 345 FDA reports)
RENAL FAILURE ( 343 FDA reports)
PRURITUS ( 333 FDA reports)
RASH ( 319 FDA reports)
RENAL FAILURE ACUTE ( 316 FDA reports)
MALAISE ( 302 FDA reports)
ASTHENIA ( 286 FDA reports)
DIARRHOEA ( 272 FDA reports)
FATIGUE ( 269 FDA reports)
SOMNOLENCE ( 261 FDA reports)
ANXIETY ( 253 FDA reports)
HEADACHE ( 249 FDA reports)
DEPRESSION ( 247 FDA reports)
BACK PAIN ( 242 FDA reports)
HYPOTENSION ( 238 FDA reports)
SUICIDE ATTEMPT ( 235 FDA reports)
CONFUSIONAL STATE ( 223 FDA reports)
WEIGHT DECREASED ( 222 FDA reports)
OEDEMA PERIPHERAL ( 221 FDA reports)
INSOMNIA ( 218 FDA reports)
DEHYDRATION ( 217 FDA reports)
THROMBOCYTOPENIA ( 212 FDA reports)
ERYTHEMA ( 208 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 206 FDA reports)
DIZZINESS ( 205 FDA reports)
TREMOR ( 197 FDA reports)
ABDOMINAL PAIN ( 195 FDA reports)
CONDITION AGGRAVATED ( 195 FDA reports)
CONVULSION ( 194 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 191 FDA reports)
HAEMOGLOBIN DECREASED ( 189 FDA reports)
PNEUMONIA ( 187 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 183 FDA reports)
DRUG INEFFECTIVE ( 183 FDA reports)
PLATELET COUNT DECREASED ( 182 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 180 FDA reports)
PLEURAL EFFUSION ( 179 FDA reports)
ARTHRALGIA ( 178 FDA reports)
WEIGHT INCREASED ( 178 FDA reports)
AGITATION ( 174 FDA reports)
DRUG INTERACTION ( 174 FDA reports)
PAIN IN EXTREMITY ( 174 FDA reports)
URTICARIA ( 174 FDA reports)
HYPERTENSION ( 172 FDA reports)
OVERDOSE ( 172 FDA reports)
TACHYCARDIA ( 172 FDA reports)
TOXIC SKIN ERUPTION ( 165 FDA reports)
CYTOLYTIC HEPATITIS ( 163 FDA reports)
CHEST PAIN ( 158 FDA reports)
DECREASED APPETITE ( 158 FDA reports)
RESPIRATORY FAILURE ( 155 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 154 FDA reports)
NEUTROPENIA ( 152 FDA reports)
BLOOD BILIRUBIN INCREASED ( 151 FDA reports)
GAIT DISTURBANCE ( 149 FDA reports)
HYPOAESTHESIA ( 147 FDA reports)
SEPSIS ( 146 FDA reports)
LOSS OF CONSCIOUSNESS ( 145 FDA reports)
ECZEMA ( 144 FDA reports)
COUGH ( 142 FDA reports)
ABNORMAL BEHAVIOUR ( 140 FDA reports)
CONSTIPATION ( 138 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 137 FDA reports)
BLOOD PRESSURE INCREASED ( 133 FDA reports)
LYMPHADENOPATHY ( 131 FDA reports)
URINARY TRACT INFECTION ( 131 FDA reports)
CARDIAC ARREST ( 127 FDA reports)
CHILLS ( 127 FDA reports)
COMA ( 127 FDA reports)
DYSPHAGIA ( 127 FDA reports)
LUNG DISORDER ( 126 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 122 FDA reports)
INFLAMMATION ( 120 FDA reports)
HYPOKALAEMIA ( 119 FDA reports)
HYPONATRAEMIA ( 118 FDA reports)
CARDIAC FAILURE ( 117 FDA reports)
OXYGEN SATURATION DECREASED ( 117 FDA reports)
VISION BLURRED ( 115 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 114 FDA reports)
HYPERSENSITIVITY ( 114 FDA reports)
BRADYCARDIA ( 113 FDA reports)
INFECTION ( 113 FDA reports)
SKIN LESION ( 112 FDA reports)
BLOOD POTASSIUM DECREASED ( 111 FDA reports)
CHOLESTASIS ( 111 FDA reports)
MUSCULAR WEAKNESS ( 111 FDA reports)
PANCYTOPENIA ( 111 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 110 FDA reports)
SUICIDAL IDEATION ( 110 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 109 FDA reports)
LIVER DISORDER ( 109 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 108 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 108 FDA reports)
ASCITES ( 107 FDA reports)
DISORIENTATION ( 106 FDA reports)
BLOOD GLUCOSE INCREASED ( 105 FDA reports)
MYOCARDIAL INFARCTION ( 105 FDA reports)
RASH MACULO-PAPULAR ( 105 FDA reports)
BLOOD CREATININE INCREASED ( 102 FDA reports)
CHEST DISCOMFORT ( 102 FDA reports)
INTERSTITIAL LUNG DISEASE ( 102 FDA reports)
SINUSITIS ( 100 FDA reports)
BRONCHITIS ( 99 FDA reports)
PULMONARY EMBOLISM ( 99 FDA reports)
DEATH ( 98 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 98 FDA reports)
MYALGIA ( 98 FDA reports)
RASH ERYTHEMATOUS ( 96 FDA reports)
RHABDOMYOLYSIS ( 96 FDA reports)
HYPERKALAEMIA ( 93 FDA reports)
INJURY ( 93 FDA reports)
NEUROPATHY PERIPHERAL ( 93 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 93 FDA reports)
ATRIAL FIBRILLATION ( 92 FDA reports)
CEREBROVASCULAR ACCIDENT ( 92 FDA reports)
SKIN EXFOLIATION ( 92 FDA reports)
ABDOMINAL PAIN UPPER ( 91 FDA reports)
BALANCE DISORDER ( 91 FDA reports)
AGGRESSION ( 90 FDA reports)
FEELING ABNORMAL ( 90 FDA reports)
DERMATITIS EXFOLIATIVE ( 89 FDA reports)
MUSCLE SPASMS ( 89 FDA reports)
JAUNDICE ( 88 FDA reports)
BLOOD PRESSURE DECREASED ( 87 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 86 FDA reports)
BONE DISORDER ( 85 FDA reports)
DYSKINESIA ( 85 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 83 FDA reports)
PALPITATIONS ( 83 FDA reports)
URINARY RETENTION ( 83 FDA reports)
HYPOGLYCAEMIA ( 82 FDA reports)
LEUKOPENIA ( 82 FDA reports)
OEDEMA ( 82 FDA reports)
RASH GENERALISED ( 81 FDA reports)
DRUG TOXICITY ( 80 FDA reports)
HYPERGLYCAEMIA ( 79 FDA reports)
MULTI-ORGAN FAILURE ( 79 FDA reports)
SHOCK ( 78 FDA reports)
EMOTIONAL DISTRESS ( 77 FDA reports)
PULMONARY OEDEMA ( 77 FDA reports)
ANAPHYLACTIC SHOCK ( 76 FDA reports)
HYPOXIA ( 76 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 76 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 75 FDA reports)
HERPES ZOSTER ( 75 FDA reports)
HYPERHIDROSIS ( 75 FDA reports)
CELLULITIS ( 74 FDA reports)
EOSINOPHILIA ( 74 FDA reports)
ANOREXIA ( 73 FDA reports)
EPISTAXIS ( 73 FDA reports)
HALLUCINATION ( 73 FDA reports)
HYPERTHERMIA ( 73 FDA reports)
OSTEOARTHRITIS ( 73 FDA reports)
PAIN IN JAW ( 73 FDA reports)
RASH PRURITIC ( 72 FDA reports)
CONTUSION ( 71 FDA reports)
ALOPECIA ( 70 FDA reports)
OSTEONECROSIS OF JAW ( 70 FDA reports)
PARAESTHESIA ( 70 FDA reports)
PSORIASIS ( 70 FDA reports)
RENAL IMPAIRMENT ( 70 FDA reports)
STEVENS-JOHNSON SYNDROME ( 70 FDA reports)
RESPIRATORY DISTRESS ( 69 FDA reports)
ANHEDONIA ( 68 FDA reports)
CARDIO-RESPIRATORY ARREST ( 68 FDA reports)
DEEP VEIN THROMBOSIS ( 68 FDA reports)
DIABETES MELLITUS ( 68 FDA reports)
DYSARTHRIA ( 68 FDA reports)
MIGRAINE ( 68 FDA reports)
OSTEOMYELITIS ( 68 FDA reports)
SYNCOPE ( 68 FDA reports)
SEPTIC SHOCK ( 67 FDA reports)
TYPE 2 DIABETES MELLITUS ( 67 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 66 FDA reports)
HEART RATE INCREASED ( 66 FDA reports)
NECK PAIN ( 66 FDA reports)
STAPHYLOCOCCAL INFECTION ( 66 FDA reports)
STOMATITIS ( 66 FDA reports)
FEBRILE NEUTROPENIA ( 65 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 65 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 64 FDA reports)
BLOOD UREA INCREASED ( 64 FDA reports)
DRUG ERUPTION ( 64 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 63 FDA reports)
IRRITABILITY ( 62 FDA reports)
JOINT SWELLING ( 62 FDA reports)
VERTIGO ( 62 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 61 FDA reports)
INFUSION RELATED REACTION ( 61 FDA reports)
INTENTIONAL OVERDOSE ( 61 FDA reports)
MALNUTRITION ( 61 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 60 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 60 FDA reports)
MUSCULOSKELETAL PAIN ( 60 FDA reports)
SWELLING ( 60 FDA reports)
CHROMATURIA ( 59 FDA reports)
DELIRIUM ( 59 FDA reports)
DRY MOUTH ( 58 FDA reports)
FACE OEDEMA ( 58 FDA reports)
DRUG HYPERSENSITIVITY ( 57 FDA reports)
HAEMORRHAGE ( 57 FDA reports)
HEPATIC FAILURE ( 57 FDA reports)
MITRAL VALVE INCOMPETENCE ( 57 FDA reports)
PURPURA ( 57 FDA reports)
CAESAREAN SECTION ( 56 FDA reports)
DEPRESSED MOOD ( 56 FDA reports)
DERMATITIS BULLOUS ( 56 FDA reports)
DISEASE PROGRESSION ( 56 FDA reports)
GASTRIC ULCER ( 56 FDA reports)
HAEMATURIA ( 56 FDA reports)
OFF LABEL USE ( 56 FDA reports)
TOOTH LOSS ( 56 FDA reports)
AGRANULOCYTOSIS ( 55 FDA reports)
CYANOSIS ( 55 FDA reports)
DISTURBANCE IN ATTENTION ( 55 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 55 FDA reports)
HEPATIC ENZYME INCREASED ( 55 FDA reports)
OSTEONECROSIS ( 55 FDA reports)
AMNESIA ( 54 FDA reports)
BRONCHOSPASM ( 54 FDA reports)
DERMATITIS ( 53 FDA reports)
HAEMATOCRIT DECREASED ( 53 FDA reports)
HEPATIC STEATOSIS ( 53 FDA reports)
NASOPHARYNGITIS ( 53 FDA reports)
RHINITIS ALLERGIC ( 53 FDA reports)
THROMBOSIS ( 53 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 53 FDA reports)
ABDOMINAL DISTENSION ( 52 FDA reports)
BLISTER ( 52 FDA reports)
DENTAL CARIES ( 52 FDA reports)
HEPATITIS ( 52 FDA reports)
PULMONARY CONGESTION ( 52 FDA reports)
RESPIRATORY DEPRESSION ( 52 FDA reports)
CORONARY ARTERY DISEASE ( 51 FDA reports)
DIALYSIS ( 51 FDA reports)
DYSPEPSIA ( 51 FDA reports)
HYPERLIPIDAEMIA ( 51 FDA reports)
IMPAIRED HEALING ( 51 FDA reports)
DRY SKIN ( 50 FDA reports)
HAEMORRHOIDS ( 50 FDA reports)
MENTAL DISORDER ( 50 FDA reports)
PNEUMONIA ASPIRATION ( 50 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 50 FDA reports)
SPEECH DISORDER ( 50 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 50 FDA reports)
ANAPHYLACTIC REACTION ( 49 FDA reports)
FUNGAL INFECTION ( 49 FDA reports)
VENTRICULAR TACHYCARDIA ( 49 FDA reports)
ASTHMA ( 48 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 48 FDA reports)
DIVERTICULUM ( 48 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 48 FDA reports)
HEPATOMEGALY ( 48 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 48 FDA reports)
SKIN ULCER ( 48 FDA reports)
TOOTH EXTRACTION ( 48 FDA reports)
ACUTE RESPIRATORY FAILURE ( 47 FDA reports)
ATELECTASIS ( 47 FDA reports)
BLOOD SODIUM DECREASED ( 47 FDA reports)
BONE PAIN ( 47 FDA reports)
ACUTE PULMONARY OEDEMA ( 46 FDA reports)
BONE MARROW FAILURE ( 46 FDA reports)
DYSGEUSIA ( 46 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 46 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 46 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 45 FDA reports)
CARDIAC DISORDER ( 45 FDA reports)
DIPLOPIA ( 45 FDA reports)
ERYTHEMA MULTIFORME ( 45 FDA reports)
LETHARGY ( 45 FDA reports)
MEDICATION ERROR ( 45 FDA reports)
OESOPHAGITIS ( 45 FDA reports)
PURULENT DISCHARGE ( 45 FDA reports)
RASH MACULAR ( 45 FDA reports)
ARRHYTHMIA ( 44 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 44 FDA reports)
HAEMATEMESIS ( 44 FDA reports)
MUSCLE RIGIDITY ( 44 FDA reports)
PULMONARY HYPERTENSION ( 44 FDA reports)
RESPIRATORY DISORDER ( 44 FDA reports)
SKIN DISORDER ( 44 FDA reports)
TRANSAMINASES INCREASED ( 44 FDA reports)
ACNE ( 43 FDA reports)
LEUKOCYTOSIS ( 43 FDA reports)
METABOLIC ACIDOSIS ( 43 FDA reports)
TOOTH FRACTURE ( 43 FDA reports)
VIRAL INFECTION ( 43 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 42 FDA reports)
MENTAL STATUS CHANGES ( 42 FDA reports)
OSTEOPOROSIS ( 42 FDA reports)
SCAR ( 42 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 42 FDA reports)
TOOTH DISORDER ( 42 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 42 FDA reports)
CANDIDIASIS ( 41 FDA reports)
DYSPNOEA EXERTIONAL ( 41 FDA reports)
GASTRITIS ( 41 FDA reports)
OROPHARYNGEAL PAIN ( 41 FDA reports)
RASH PAPULAR ( 41 FDA reports)
SPINAL OSTEOARTHRITIS ( 41 FDA reports)
TACHYPNOEA ( 41 FDA reports)
CATARACT ( 40 FDA reports)
DEFORMITY ( 40 FDA reports)
DISCOMFORT ( 40 FDA reports)
DRUG DEPENDENCE ( 40 FDA reports)
INFLUENZA LIKE ILLNESS ( 40 FDA reports)
NEUTROPHIL COUNT DECREASED ( 40 FDA reports)
PANCREATITIS ( 40 FDA reports)
RENAL DISORDER ( 40 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 40 FDA reports)
URINARY INCONTINENCE ( 40 FDA reports)
CHOLELITHIASIS ( 39 FDA reports)
GINGIVAL PAIN ( 39 FDA reports)
PANCREATITIS ACUTE ( 39 FDA reports)
PREMATURE BABY ( 39 FDA reports)
ARTHRITIS ( 38 FDA reports)
BODY TEMPERATURE INCREASED ( 38 FDA reports)
CARDIOMEGALY ( 38 FDA reports)
CARDIOMYOPATHY ( 38 FDA reports)
GENERALISED OEDEMA ( 38 FDA reports)
HIATUS HERNIA ( 38 FDA reports)
HYPOVENTILATION ( 38 FDA reports)
PERICARDIAL EFFUSION ( 38 FDA reports)
PRURIGO ( 38 FDA reports)
RECTAL HAEMORRHAGE ( 38 FDA reports)
RESPIRATORY ARREST ( 38 FDA reports)
TREATMENT NONCOMPLIANCE ( 38 FDA reports)
AKINESIA ( 37 FDA reports)
COMPULSIVE SHOPPING ( 37 FDA reports)
DYSURIA ( 37 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 37 FDA reports)
MEMORY IMPAIRMENT ( 37 FDA reports)
PNEUMOTHORAX ( 37 FDA reports)
RASH PUSTULAR ( 37 FDA reports)
SLEEP APNOEA SYNDROME ( 37 FDA reports)
EOSINOPHIL COUNT INCREASED ( 36 FDA reports)
FISTULA ( 36 FDA reports)
GINGIVAL RECESSION ( 36 FDA reports)
HAEMATOMA ( 36 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 36 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 36 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 36 FDA reports)
OBESITY ( 36 FDA reports)
PRURITUS GENERALISED ( 36 FDA reports)
RENAL FAILURE CHRONIC ( 36 FDA reports)
STRESS ( 36 FDA reports)
TOOTH INFECTION ( 36 FDA reports)
TORSADE DE POINTES ( 36 FDA reports)
HYPOTHYROIDISM ( 35 FDA reports)
INJECTION SITE NECROSIS ( 35 FDA reports)
LYMPHOPENIA ( 35 FDA reports)
NEOPLASM MALIGNANT ( 35 FDA reports)
OLIGURIA ( 35 FDA reports)
ORTHOSTATIC HYPOTENSION ( 35 FDA reports)
SLEEP DISORDER ( 35 FDA reports)
VISUAL ACUITY REDUCED ( 35 FDA reports)
BLOOD GLUCOSE DECREASED ( 34 FDA reports)
BLOOD POTASSIUM INCREASED ( 34 FDA reports)
CARDIAC MURMUR ( 34 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 34 FDA reports)
ENCEPHALOPATHY ( 34 FDA reports)
ESCHERICHIA INFECTION ( 34 FDA reports)
GENERALISED ERYTHEMA ( 34 FDA reports)
INTESTINAL OBSTRUCTION ( 34 FDA reports)
LICHENOID KERATOSIS ( 34 FDA reports)
NERVOUSNESS ( 34 FDA reports)
NIGHT SWEATS ( 34 FDA reports)
PRIMARY SEQUESTRUM ( 34 FDA reports)
SINUS TACHYCARDIA ( 34 FDA reports)
ABSCESS ( 33 FDA reports)
ANGINA PECTORIS ( 33 FDA reports)
ANGIOEDEMA ( 33 FDA reports)
COMPLETED SUICIDE ( 33 FDA reports)
HEPATITIS CHOLESTATIC ( 33 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 33 FDA reports)
HYPERCHOLESTEROLAEMIA ( 33 FDA reports)
HYPOMANIA ( 33 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 33 FDA reports)
OSTEOPENIA ( 33 FDA reports)
SWELLING FACE ( 33 FDA reports)
CIRCULATORY COLLAPSE ( 32 FDA reports)
CORNEAL REFLEX DECREASED ( 32 FDA reports)
DEMENTIA ( 32 FDA reports)
LARYNGEAL OEDEMA ( 32 FDA reports)
METASTASES TO BONE ( 32 FDA reports)
PSYCHOTIC BEHAVIOUR ( 32 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 32 FDA reports)
RHINORRHOEA ( 32 FDA reports)
SEDATION ( 32 FDA reports)
ACTINOMYCOSIS ( 31 FDA reports)
AMIMIA ( 31 FDA reports)
CEREBRAL HAEMORRHAGE ( 31 FDA reports)
CHOLANGITIS ( 31 FDA reports)
DEBRIDEMENT ( 31 FDA reports)
EAR PAIN ( 31 FDA reports)
INJECTION SITE ULCER ( 31 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 31 FDA reports)
RESTLESSNESS ( 31 FDA reports)
THYMUS DISORDER ( 31 FDA reports)
DYSPHONIA ( 30 FDA reports)
EPILEPSY ( 30 FDA reports)
GINGIVAL BLEEDING ( 30 FDA reports)
GINGIVAL SWELLING ( 30 FDA reports)
HEAD INJURY ( 30 FDA reports)
HYPERVENTILATION ( 30 FDA reports)
LIPASE INCREASED ( 30 FDA reports)
MELAENA ( 30 FDA reports)
MULTIPLE MYELOMA ( 30 FDA reports)
PNEUMONITIS ( 30 FDA reports)
RIB FRACTURE ( 30 FDA reports)
APHASIA ( 29 FDA reports)
BACTERIAL INFECTION ( 29 FDA reports)
BLOOD ALBUMIN DECREASED ( 29 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 29 FDA reports)
HEPATITIS FULMINANT ( 29 FDA reports)
HYPOTONIA ( 29 FDA reports)
MYCOSIS FUNGOIDES ( 29 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 29 FDA reports)
SHOCK HAEMORRHAGIC ( 29 FDA reports)
ANURIA ( 28 FDA reports)
CERUMEN IMPACTION ( 28 FDA reports)
DEVICE RELATED INFECTION ( 28 FDA reports)
DIABETIC NEUROPATHY ( 28 FDA reports)
HALLUCINATION, VISUAL ( 28 FDA reports)
INJECTION SITE PAIN ( 28 FDA reports)
LIVER INJURY ( 28 FDA reports)
LOOSE TOOTH ( 28 FDA reports)
MASS ( 28 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 28 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 28 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 28 FDA reports)
PLATELET COUNT INCREASED ( 28 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 27 FDA reports)
CYST ( 27 FDA reports)
DRUG EFFECT DECREASED ( 27 FDA reports)
GASTROINTESTINAL DISORDER ( 27 FDA reports)
GRAND MAL CONVULSION ( 27 FDA reports)
HEPATITIS ACUTE ( 27 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 27 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 27 FDA reports)
PHOTOSENSITIVITY REACTION ( 27 FDA reports)
PROTEIN TOTAL DECREASED ( 27 FDA reports)
SUBDURAL HAEMATOMA ( 27 FDA reports)
VAGINAL HAEMORRHAGE ( 27 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 27 FDA reports)
BONE NEOPLASM MALIGNANT ( 26 FDA reports)
DERMATITIS ALLERGIC ( 26 FDA reports)
EAR INFECTION ( 26 FDA reports)
EJECTION FRACTION DECREASED ( 26 FDA reports)
HEART RATE DECREASED ( 26 FDA reports)
ILEUS ( 26 FDA reports)
PALLOR ( 26 FDA reports)
POST PROCEDURAL COMPLICATION ( 26 FDA reports)
SPINAL COMPRESSION FRACTURE ( 26 FDA reports)
ACCIDENTAL OVERDOSE ( 25 FDA reports)
AORTIC VALVE INCOMPETENCE ( 25 FDA reports)
BONE DENSITY DECREASED ( 25 FDA reports)
CONJUNCTIVITIS ( 25 FDA reports)
DERMATITIS CONTACT ( 25 FDA reports)
DRY EYE ( 25 FDA reports)
ECONOMIC PROBLEM ( 25 FDA reports)
FIBROMYALGIA ( 25 FDA reports)
HAEMODIALYSIS ( 25 FDA reports)
HYPERBILIRUBINAEMIA ( 25 FDA reports)
HYPOALBUMINAEMIA ( 25 FDA reports)
HYPOPHAGIA ( 25 FDA reports)
LUNG INFECTION ( 25 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 25 FDA reports)
MYDRIASIS ( 25 FDA reports)
NEOPLASM ( 25 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 25 FDA reports)
PRODUCTIVE COUGH ( 25 FDA reports)
RASH MORBILLIFORM ( 25 FDA reports)
ROAD TRAFFIC ACCIDENT ( 25 FDA reports)
SKIN HYPERPIGMENTATION ( 25 FDA reports)
THIRST ( 25 FDA reports)
TOOTHACHE ( 25 FDA reports)
ASPIRATION ( 24 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
DISEASE RECURRENCE ( 24 FDA reports)
DRUG ABUSER ( 24 FDA reports)
EMPHYSEMA ( 24 FDA reports)
EYELID OEDEMA ( 24 FDA reports)
FLATULENCE ( 24 FDA reports)
HAEMODYNAMIC INSTABILITY ( 24 FDA reports)
MANIA ( 24 FDA reports)
MOBILITY DECREASED ( 24 FDA reports)
MYOCARDIAL ISCHAEMIA ( 24 FDA reports)
MYOCLONUS ( 24 FDA reports)
NEPHROLITHIASIS ( 24 FDA reports)
NERVOUS SYSTEM DISORDER ( 24 FDA reports)
ORAL DISORDER ( 24 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 24 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 24 FDA reports)
ACIDOSIS ( 23 FDA reports)
BLOOD CHLORIDE DECREASED ( 23 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 23 FDA reports)
BURNING SENSATION ( 23 FDA reports)
CATHETERISATION CARDIAC ( 23 FDA reports)
COGNITIVE DISORDER ( 23 FDA reports)
DYSTHYMIC DISORDER ( 23 FDA reports)
EATING DISORDER ( 23 FDA reports)
GINGIVITIS ( 23 FDA reports)
HYPERPLASIA ( 23 FDA reports)
INCORRECT DOSE ADMINISTERED ( 23 FDA reports)
KYPHOSIS ( 23 FDA reports)
LOGORRHOEA ( 23 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 23 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 23 FDA reports)
NEUROBLASTOMA RECURRENT ( 23 FDA reports)
PARANOIA ( 23 FDA reports)
PETECHIAE ( 23 FDA reports)
PREGNANCY ( 23 FDA reports)
RALES ( 23 FDA reports)
SINUS BRADYCARDIA ( 23 FDA reports)
WITHDRAWAL SYNDROME ( 23 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 22 FDA reports)
CHEST X-RAY ABNORMAL ( 22 FDA reports)
DYSLIPIDAEMIA ( 22 FDA reports)
FLUID RETENTION ( 22 FDA reports)
FOLLICULITIS ( 22 FDA reports)
GRAFT VERSUS HOST DISEASE ( 22 FDA reports)
HODGKIN'S DISEASE ( 22 FDA reports)
ILEUS PARALYTIC ( 22 FDA reports)
LACERATION ( 22 FDA reports)
MUCOUS MEMBRANE DISORDER ( 22 FDA reports)
MULTIPLE DRUG OVERDOSE ( 22 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 22 FDA reports)
PHYSICAL DISABILITY ( 22 FDA reports)
PYELONEPHRITIS ( 22 FDA reports)
RENAL CYST ( 22 FDA reports)
SKIN CANCER ( 22 FDA reports)
SKIN DISCOLOURATION ( 22 FDA reports)
SKIN NECROSIS ( 22 FDA reports)
SUDDEN DEATH ( 22 FDA reports)
VENTRICULAR FIBRILLATION ( 22 FDA reports)
ALCOHOL USE ( 21 FDA reports)
APATHY ( 21 FDA reports)
BASAL CELL CARCINOMA ( 21 FDA reports)
BLOOD AMYLASE INCREASED ( 21 FDA reports)
BLOOD PRESSURE ABNORMAL ( 21 FDA reports)
BLOOD URINE PRESENT ( 21 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 21 FDA reports)
CHOKING ( 21 FDA reports)
DERMATOMYOSITIS ( 21 FDA reports)
DIVERTICULITIS ( 21 FDA reports)
ECCHYMOSIS ( 21 FDA reports)
EYE PAIN ( 21 FDA reports)
FEELING COLD ( 21 FDA reports)
FEELING HOT ( 21 FDA reports)
GASTROENTERITIS ( 21 FDA reports)
HYPOTHERMIA ( 21 FDA reports)
HYPOTONIA NEONATAL ( 21 FDA reports)
INCREASED APPETITE ( 21 FDA reports)
IRON DEFICIENCY ( 21 FDA reports)
LUNG NEOPLASM MALIGNANT ( 21 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 21 FDA reports)
MOUTH ULCERATION ( 21 FDA reports)
PEMPHIGOID ( 21 FDA reports)
PHARYNGITIS ( 21 FDA reports)
PRESBYOPIA ( 21 FDA reports)
PROCEDURAL PAIN ( 21 FDA reports)
PROTHROMBIN TIME PROLONGED ( 21 FDA reports)
RENAL TUBULAR NECROSIS ( 21 FDA reports)
SENSORY DISTURBANCE ( 21 FDA reports)
VISUAL IMPAIRMENT ( 21 FDA reports)
ABORTION INDUCED ( 20 FDA reports)
CRYING ( 20 FDA reports)
FOOT FRACTURE ( 20 FDA reports)
HEPATIC ENCEPHALOPATHY ( 20 FDA reports)
HERPES SIMPLEX ( 20 FDA reports)
HYPERNATRAEMIA ( 20 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 20 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 20 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 20 FDA reports)
PAIN OF SKIN ( 20 FDA reports)
PERIODONTITIS ( 20 FDA reports)
RESTLESS LEGS SYNDROME ( 20 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 20 FDA reports)
WHEEZING ( 20 FDA reports)
ANAPHYLACTOID REACTION ( 19 FDA reports)
ANGIONEUROTIC OEDEMA ( 19 FDA reports)
BURSITIS ( 19 FDA reports)
COLITIS ISCHAEMIC ( 19 FDA reports)
DEAFNESS ( 19 FDA reports)
DRUG INTOLERANCE ( 19 FDA reports)
EMOTIONAL DISORDER ( 19 FDA reports)
FLUSHING ( 19 FDA reports)
FOETAL GROWTH RETARDATION ( 19 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 19 FDA reports)
HYPERTONIA ( 19 FDA reports)
LIVER TRANSPLANT REJECTION ( 19 FDA reports)
MULTIPLE ALLERGIES ( 19 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 19 FDA reports)
ORAL CAVITY FISTULA ( 19 FDA reports)
ORAL HERPES ( 19 FDA reports)
OSTEITIS ( 19 FDA reports)
PANIC ATTACK ( 19 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 19 FDA reports)
RESPIRATORY ACIDOSIS ( 19 FDA reports)
TONGUE OEDEMA ( 19 FDA reports)
VASCULITIS ( 19 FDA reports)
VENTRICULAR HYPERTROPHY ( 19 FDA reports)
WOUND DRAINAGE ( 19 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 18 FDA reports)
CACHEXIA ( 18 FDA reports)
CARDIOVASCULAR DISORDER ( 18 FDA reports)
DIVERTICULUM INTESTINAL ( 18 FDA reports)
ENDODONTIC PROCEDURE ( 18 FDA reports)
EPIDERMAL NECROSIS ( 18 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 18 FDA reports)
FIBROSIS ( 18 FDA reports)
GINGIVAL ULCERATION ( 18 FDA reports)
HAEMANGIOMA ( 18 FDA reports)
HALLUCINATION, AUDITORY ( 18 FDA reports)
HEART RATE IRREGULAR ( 18 FDA reports)
HEPATITIS C ( 18 FDA reports)
HOSPITALISATION ( 18 FDA reports)
HOT FLUSH ( 18 FDA reports)
HYPERAESTHESIA ( 18 FDA reports)
HYPERAMMONAEMIA ( 18 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 18 FDA reports)
INJECTION SITE HAEMATOMA ( 18 FDA reports)
INJECTION SITE INDURATION ( 18 FDA reports)
INTENTIONAL DRUG MISUSE ( 18 FDA reports)
JOINT SPRAIN ( 18 FDA reports)
JOINT STIFFNESS ( 18 FDA reports)
MAJOR DEPRESSION ( 18 FDA reports)
MUCOSAL INFLAMMATION ( 18 FDA reports)
ORAL DISCOMFORT ( 18 FDA reports)
PHOTOPHERESIS ( 18 FDA reports)
PROTEINURIA ( 18 FDA reports)
RASH VESICULAR ( 18 FDA reports)
SKIN INDURATION ( 18 FDA reports)
SUBILEUS ( 18 FDA reports)
UNEVALUABLE EVENT ( 18 FDA reports)
WOUND INFECTION ( 18 FDA reports)
ABSCESS JAW ( 17 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 17 FDA reports)
BONE LOSS ( 17 FDA reports)
CEREBRAL INFARCTION ( 17 FDA reports)
CEREBRAL ISCHAEMIA ( 17 FDA reports)
COLLAPSE OF LUNG ( 17 FDA reports)
DENTAL PROSTHESIS USER ( 17 FDA reports)
DIASTOLIC DYSFUNCTION ( 17 FDA reports)
DRUG LEVEL INCREASED ( 17 FDA reports)
DYSPAREUNIA ( 17 FDA reports)
EYE DISORDER ( 17 FDA reports)
FEAR ( 17 FDA reports)
FURUNCLE ( 17 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 17 FDA reports)
INJECTION SITE ERYTHEMA ( 17 FDA reports)
JAW DISORDER ( 17 FDA reports)
KLEBSIELLA INFECTION ( 17 FDA reports)
LACRIMATION INCREASED ( 17 FDA reports)
LIFE EXPECTANCY SHORTENED ( 17 FDA reports)
MOVEMENT DISORDER ( 17 FDA reports)
MYOPATHY ( 17 FDA reports)
NEONATAL DISORDER ( 17 FDA reports)
NEURALGIA ( 17 FDA reports)
NIGHTMARE ( 17 FDA reports)
PAPILLOMA ( 17 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 17 FDA reports)
PROCTALGIA ( 17 FDA reports)
RHEUMATOID ARTHRITIS ( 17 FDA reports)
SKIN PLAQUE ( 17 FDA reports)
UTERINE LEIOMYOMA ( 17 FDA reports)
VENOOCCLUSIVE DISEASE ( 17 FDA reports)
VENOUS THROMBOSIS ( 17 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 16 FDA reports)
AORTIC ANEURYSM ( 16 FDA reports)
AORTIC CALCIFICATION ( 16 FDA reports)
ASTIGMATISM ( 16 FDA reports)
AXONAL NEUROPATHY ( 16 FDA reports)
BACTERIAL SEPSIS ( 16 FDA reports)
BRADYPNOEA ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
CEREBRAL ATROPHY ( 16 FDA reports)
CHOLECYSTECTOMY ( 16 FDA reports)
COLITIS ( 16 FDA reports)
COLONIC POLYP ( 16 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 16 FDA reports)
FAILURE TO THRIVE ( 16 FDA reports)
FIBULA FRACTURE ( 16 FDA reports)
GINGIVAL ERYTHEMA ( 16 FDA reports)
HAEMOLYSIS ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 16 FDA reports)
HAND FRACTURE ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
LUPUS-LIKE SYNDROME ( 16 FDA reports)
LYMPHADENITIS ( 16 FDA reports)
MAMMOGRAM ABNORMAL ( 16 FDA reports)
NEOPLASM PROGRESSION ( 16 FDA reports)
NEUROSIS ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
PERIPHERAL COLDNESS ( 16 FDA reports)
PYELOCALIECTASIS ( 16 FDA reports)
SKIN FIBROSIS ( 16 FDA reports)
SKIN HYPERTROPHY ( 16 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 16 FDA reports)
THERAPY NON-RESPONDER ( 16 FDA reports)
THORACOTOMY ( 16 FDA reports)
TOOTH DEPOSIT ( 16 FDA reports)
VENTRICULAR ARRHYTHMIA ( 16 FDA reports)
ANORECTAL DISCOMFORT ( 15 FDA reports)
ARTERIOSCLEROSIS ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
COAGULOPATHY ( 15 FDA reports)
CORONARY ANGIOPLASTY ( 15 FDA reports)
DERMATITIS ATOPIC ( 15 FDA reports)
DUODENITIS ( 15 FDA reports)
FEBRILE BONE MARROW APLASIA ( 15 FDA reports)
FEMUR FRACTURE ( 15 FDA reports)
GASTROINTESTINAL ULCER ( 15 FDA reports)
GLAUCOMA ( 15 FDA reports)
HAEMATOCHEZIA ( 15 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
HEPATOCELLULAR INJURY ( 15 FDA reports)
HYPOCALCAEMIA ( 15 FDA reports)
KELOID SCAR ( 15 FDA reports)
LACUNAR INFARCTION ( 15 FDA reports)
LARYNGOCELE ( 15 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
MASTOCYTOSIS ( 15 FDA reports)
OLIGOHYDRAMNIOS ( 15 FDA reports)
ORAL INTAKE REDUCED ( 15 FDA reports)
PHOTOPHOBIA ( 15 FDA reports)
POLLAKIURIA ( 15 FDA reports)
POLYURIA ( 15 FDA reports)
PREMATURE LABOUR ( 15 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 15 FDA reports)
PSEUDOMONAS INFECTION ( 15 FDA reports)
PSYCHOTIC DISORDER ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA ( 15 FDA reports)
SWOLLEN TONGUE ( 15 FDA reports)
TOOTH ABSCESS ( 15 FDA reports)
TREMOR NEONATAL ( 15 FDA reports)
ULCER ( 15 FDA reports)
VITREOUS FLOATERS ( 15 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 14 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
ANGIOPATHY ( 14 FDA reports)
APNOEA ( 14 FDA reports)
BLADDER DILATATION ( 14 FDA reports)
BLOOD IRON DECREASED ( 14 FDA reports)
BONE LESION ( 14 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 14 FDA reports)
DECUBITUS ULCER ( 14 FDA reports)
DENTAL OPERATION ( 14 FDA reports)
DERMAL CYST ( 14 FDA reports)
DRUG ADMINISTRATION ERROR ( 14 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 14 FDA reports)
EXOSTOSIS ( 14 FDA reports)
FLUID OVERLOAD ( 14 FDA reports)
GALLBLADDER DISORDER ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
HYPERCAPNIA ( 14 FDA reports)
HYPERURICAEMIA ( 14 FDA reports)
ILL-DEFINED DISORDER ( 14 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 14 FDA reports)
INCOHERENT ( 14 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 14 FDA reports)
JAUNDICE NEONATAL ( 14 FDA reports)
JAW OPERATION ( 14 FDA reports)
LUNG NEOPLASM ( 14 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 14 FDA reports)
METASTASES TO LIVER ( 14 FDA reports)
MUSCLE TWITCHING ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
NASAL SEPTUM DEVIATION ( 14 FDA reports)
NO THERAPEUTIC RESPONSE ( 14 FDA reports)
ONYCHOMYCOSIS ( 14 FDA reports)
OSTEOLYSIS ( 14 FDA reports)
PROCEDURAL COMPLICATION ( 14 FDA reports)
RADIATION SKIN INJURY ( 14 FDA reports)
REFLUX LARYNGITIS ( 14 FDA reports)
SELF-MEDICATION ( 14 FDA reports)
SENSITIVITY OF TEETH ( 14 FDA reports)
SERUM SICKNESS ( 14 FDA reports)
SKIN TEST POSITIVE ( 14 FDA reports)
SKIN TIGHTNESS ( 14 FDA reports)
SPLENOMEGALY ( 14 FDA reports)
TALIPES ( 14 FDA reports)
TENDERNESS ( 14 FDA reports)
THROAT IRRITATION ( 14 FDA reports)
VASCULAR PURPURA ( 14 FDA reports)
ABDOMINAL DISCOMFORT ( 13 FDA reports)
ABORTION SPONTANEOUS ( 13 FDA reports)
ADRENAL INSUFFICIENCY ( 13 FDA reports)
ALCOHOLISM ( 13 FDA reports)
ANOGENITAL WARTS ( 13 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 13 FDA reports)
BACTERIAL TEST POSITIVE ( 13 FDA reports)
BIPOLAR DISORDER ( 13 FDA reports)
BLOOD CULTURE POSITIVE ( 13 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 13 FDA reports)
CERVICAL SPINAL STENOSIS ( 13 FDA reports)
CHEILITIS ( 13 FDA reports)
COLD SWEAT ( 13 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 13 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 13 FDA reports)
CREPITATIONS ( 13 FDA reports)
CYSTITIS ( 13 FDA reports)
DELUSION ( 13 FDA reports)
DENTURE WEARER ( 13 FDA reports)
DEVICE LEAKAGE ( 13 FDA reports)
DIABETES INSIPIDUS ( 13 FDA reports)
EAR CONGESTION ( 13 FDA reports)
EDENTULOUS ( 13 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 13 FDA reports)
FEEDING DISORDER NEONATAL ( 13 FDA reports)
FLANK PAIN ( 13 FDA reports)
GENITAL HERPES ( 13 FDA reports)
GLOSSITIS ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
HEPATIC NECROSIS ( 13 FDA reports)
HERNIA ( 13 FDA reports)
HYPOCHLORAEMIA ( 13 FDA reports)
HYPOPHOSPHATAEMIA ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
INTESTINAL DILATATION ( 13 FDA reports)
INTRA-UTERINE DEATH ( 13 FDA reports)
LOCALISED INFECTION ( 13 FDA reports)
LOCALISED OEDEMA ( 13 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 13 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 13 FDA reports)
MUSCLE HAEMORRHAGE ( 13 FDA reports)
NECROSIS ( 13 FDA reports)
NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
NOSOCOMIAL INFECTION ( 13 FDA reports)
ORAL SURGERY ( 13 FDA reports)
PERICARDITIS ( 13 FDA reports)
PHOTOPSIA ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
SNORING ( 13 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
SURGERY ( 13 FDA reports)
THROMBOPHLEBITIS ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
ANGER ( 12 FDA reports)
ANXIETY DISORDER ( 12 FDA reports)
BEHCET'S SYNDROME ( 12 FDA reports)
BONE DEBRIDEMENT ( 12 FDA reports)
BONE SWELLING ( 12 FDA reports)
CARDIAC FAILURE ACUTE ( 12 FDA reports)
CHOLECYSTITIS CHRONIC ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 12 FDA reports)
CORONARY ARTERY STENOSIS ( 12 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 12 FDA reports)
DIABETIC KETOACIDOSIS ( 12 FDA reports)
DROP ATTACKS ( 12 FDA reports)
DRUG ABUSE ( 12 FDA reports)
DRUG SCREEN POSITIVE ( 12 FDA reports)
ECZEMA INFECTED ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 12 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 12 FDA reports)
ELECTROLYTE IMBALANCE ( 12 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 12 FDA reports)
FOETAL ARRHYTHMIA ( 12 FDA reports)
FOETAL DISTRESS SYNDROME ( 12 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 12 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 12 FDA reports)
GINGIVAL OEDEMA ( 12 FDA reports)
GOUT ( 12 FDA reports)
HEPATOCELLULAR DAMAGE ( 12 FDA reports)
HYPERTHERMIA MALIGNANT ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
HYPOVOLAEMIA ( 12 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 12 FDA reports)
INJECTION SITE REACTION ( 12 FDA reports)
INTERVERTEBRAL DISCITIS ( 12 FDA reports)
LACTIC ACIDOSIS ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LIMB INJURY ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
LYMPHOCYTIC INFILTRATION ( 12 FDA reports)
MALIGNANT TUMOUR EXCISION ( 12 FDA reports)
MITRAL VALVE PROLAPSE ( 12 FDA reports)
MONOPLEGIA ( 12 FDA reports)
MUSCULOSKELETAL DISORDER ( 12 FDA reports)
MYELODYSPLASTIC SYNDROME ( 12 FDA reports)
NEOPLASM RECURRENCE ( 12 FDA reports)
ORAL PAIN ( 12 FDA reports)
PANCREATITIS CHRONIC ( 12 FDA reports)
PARALYSIS ( 12 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
POLYDIPSIA ( 12 FDA reports)
POOR DENTAL CONDITION ( 12 FDA reports)
PYODERMA GANGRENOSUM ( 12 FDA reports)
RADIOTHERAPY TO BRAIN ( 12 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 12 FDA reports)
STATUS EPILEPTICUS ( 12 FDA reports)
STILLBIRTH ( 12 FDA reports)
TARDIVE DYSKINESIA ( 12 FDA reports)
TENDONITIS ( 12 FDA reports)
TINNITUS ( 12 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 12 FDA reports)
ABNORMAL DREAMS ( 11 FDA reports)
ANOXIC ENCEPHALOPATHY ( 11 FDA reports)
ARTHROPATHY ( 11 FDA reports)
ATAXIA ( 11 FDA reports)
AUTOIMMUNE HEPATITIS ( 11 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 11 FDA reports)
BILE DUCT OBSTRUCTION ( 11 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 11 FDA reports)
CAROTID ARTERY DISEASE ( 11 FDA reports)
COMPRESSION FRACTURE ( 11 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 11 FDA reports)
ERYSIPELAS ( 11 FDA reports)
FACIAL PALSY ( 11 FDA reports)
FORMICATION ( 11 FDA reports)
GALACTORRHOEA ( 11 FDA reports)
GASTROINTESTINAL PAIN ( 11 FDA reports)
GINGIVAL INFECTION ( 11 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 11 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 11 FDA reports)
INFLUENZA ( 11 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 11 FDA reports)
ISCHAEMIC STROKE ( 11 FDA reports)
LENTIGO ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
LUNG INFILTRATION ( 11 FDA reports)
MICROCYTIC ANAEMIA ( 11 FDA reports)
MICTURITION URGENCY ( 11 FDA reports)
MOOD ALTERED ( 11 FDA reports)
MUSCLE CONTRACTURE ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
NIKOLSKY'S SIGN ( 11 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 11 FDA reports)
OVARIAN CANCER ( 11 FDA reports)
PARAESTHESIA ORAL ( 11 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 11 FDA reports)
PHARYNGEAL OEDEMA ( 11 FDA reports)
POST HERPETIC NEURALGIA ( 11 FDA reports)
PSORIATIC ARTHROPATHY ( 11 FDA reports)
PULMONARY FIBROSIS ( 11 FDA reports)
RESPIRATORY RATE DECREASED ( 11 FDA reports)
SEBORRHOEIC DERMATITIS ( 11 FDA reports)
SKIN BURNING SENSATION ( 11 FDA reports)
SKIN INFECTION ( 11 FDA reports)
SKIN PAPILLOMA ( 11 FDA reports)
SOFT TISSUE DISORDER ( 11 FDA reports)
STRIDOR ( 11 FDA reports)
SUICIDAL BEHAVIOUR ( 11 FDA reports)
SYNOVIAL CYST ( 11 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
UTERINE POLYP ( 11 FDA reports)
VAGINAL INFECTION ( 11 FDA reports)
WHEELCHAIR USER ( 11 FDA reports)
ABDOMINAL PAIN LOWER ( 10 FDA reports)
ALLERGY TO ANIMAL ( 10 FDA reports)
ALVEOLITIS ( 10 FDA reports)
ANAESTHETIC COMPLICATION ( 10 FDA reports)
ANAPHYLACTOID SHOCK ( 10 FDA reports)
APLASIA ( 10 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 10 FDA reports)
BLOOD OSMOLARITY DECREASED ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BLOOD PROLACTIN INCREASED ( 10 FDA reports)
BREAST CANCER IN SITU ( 10 FDA reports)
BREATH ODOUR ( 10 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 10 FDA reports)
CARDIAC VALVE SCLEROSIS ( 10 FDA reports)
CATARACT OPERATION ( 10 FDA reports)
CEREBRAL HAEMATOMA ( 10 FDA reports)
CHOLECYSTITIS ACUTE ( 10 FDA reports)
DENTAL FISTULA ( 10 FDA reports)
DIFFICULTY IN WALKING ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
DYSSTASIA ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 10 FDA reports)
EXCORIATION ( 10 FDA reports)
EYE MOVEMENT DISORDER ( 10 FDA reports)
FEELING OF DESPAIR ( 10 FDA reports)
FISTULA REPAIR ( 10 FDA reports)
FOETAL MOVEMENTS DECREASED ( 10 FDA reports)
HEPATORENAL SYNDROME ( 10 FDA reports)
HYPERKERATOSIS ( 10 FDA reports)
HYPERLACTACIDAEMIA ( 10 FDA reports)
HYPOPNOEA ( 10 FDA reports)
IMPULSIVE BEHAVIOUR ( 10 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 10 FDA reports)
INJECTION SITE HAEMORRHAGE ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
JAUNDICE CHOLESTATIC ( 10 FDA reports)
KIDNEY INFECTION ( 10 FDA reports)
KYPHOSCOLIOSIS ( 10 FDA reports)
LUNG HYPERINFLATION ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MENISCUS LESION ( 10 FDA reports)
METABOLIC ENCEPHALOPATHY ( 10 FDA reports)
METASTASES TO OVARY ( 10 FDA reports)
MIXED LIVER INJURY ( 10 FDA reports)
MYOPIA ( 10 FDA reports)
NASAL POLYPS ( 10 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 10 FDA reports)
OOPHORECTOMY ( 10 FDA reports)
PANCREATIC CARCINOMA ( 10 FDA reports)
PAPILLOMA VIRAL INFECTION ( 10 FDA reports)
PATHOLOGICAL FRACTURE ( 10 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 10 FDA reports)
PLACENTAL DISORDER ( 10 FDA reports)
PLASMACYTOSIS ( 10 FDA reports)
PLASTIC SURGERY TO THE FACE ( 10 FDA reports)
PORTAL VEIN THROMBOSIS ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PULSE ABSENT ( 10 FDA reports)
RADIOTHERAPY ( 10 FDA reports)
RESPIRATORY RATE INCREASED ( 10 FDA reports)
SALIVARY HYPERSECRETION ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SINUS POLYP ( 10 FDA reports)
SKIN FRAGILITY ( 10 FDA reports)
SKIN INFLAMMATION ( 10 FDA reports)
SPINA BIFIDA ( 10 FDA reports)
SUBCUTANEOUS NODULE ( 10 FDA reports)
SUBMANDIBULAR MASS ( 10 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 10 FDA reports)
T-CELL LYMPHOMA ( 10 FDA reports)
TONGUE DISCOLOURATION ( 10 FDA reports)
TRYPTASE INCREASED ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ABSCESS INTESTINAL ( 9 FDA reports)
ADHESIOLYSIS ( 9 FDA reports)
ALVEOLOPLASTY ( 9 FDA reports)
ANGIOMYOLIPOMA ( 9 FDA reports)
APLASTIC ANAEMIA ( 9 FDA reports)
AREFLEXIA ( 9 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BIPOLAR I DISORDER ( 9 FDA reports)
BLOOD CALCIUM DECREASED ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 9 FDA reports)
BODY TEMPERATURE DECREASED ( 9 FDA reports)
BREAST MASS ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
CARDIOPULMONARY FAILURE ( 9 FDA reports)
CARPAL TUNNEL SYNDROME ( 9 FDA reports)
CATHETER RELATED INFECTION ( 9 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 9 FDA reports)
COLON ADENOMA ( 9 FDA reports)
CORONARY ARTERY RESTENOSIS ( 9 FDA reports)
CULTURE URINE POSITIVE ( 9 FDA reports)
DEVICE MALFUNCTION ( 9 FDA reports)
DIABETIC COMA ( 9 FDA reports)
DISSOCIATIVE FUGUE ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 9 FDA reports)
ENTEROCOLITIS ( 9 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 9 FDA reports)
ERECTILE DYSFUNCTION ( 9 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
FAECALOMA ( 9 FDA reports)
FAECES DISCOLOURED ( 9 FDA reports)
FAECES PALE ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
FRUSTRATION ( 9 FDA reports)
GASTRIC CANCER ( 9 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
ILLUSION ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
INTERMITTENT CLAUDICATION ( 9 FDA reports)
JAW FRACTURE ( 9 FDA reports)
JOINT INJURY ( 9 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
METASTASES TO SPINE ( 9 FDA reports)
MIOSIS ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MULTIPLE INJURIES ( 9 FDA reports)
MUSCLE CRAMP ( 9 FDA reports)
MUSCLE STRAIN ( 9 FDA reports)
MUSCLE TIGHTNESS ( 9 FDA reports)
NAIL DISORDER ( 9 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 9 FDA reports)
ODYNOPHAGIA ( 9 FDA reports)
OESOPHAGEAL STENOSIS ( 9 FDA reports)
ORAL CANDIDIASIS ( 9 FDA reports)
OTITIS MEDIA ( 9 FDA reports)
PALATAL DISORDER ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PELVIC ABSCESS ( 9 FDA reports)
PERITONITIS ( 9 FDA reports)
PHYSICAL ASSAULT ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 9 FDA reports)
PSEUDOMONAL SEPSIS ( 9 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 9 FDA reports)
PULMONARY TUBERCULOSIS ( 9 FDA reports)
RENAL TUBULAR DISORDER ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
RETCHING ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
SARCOIDOSIS ( 9 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 9 FDA reports)
SKIN REACTION ( 9 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
TUMOUR LYSIS SYNDROME ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
VITREOUS HAEMORRHAGE ( 9 FDA reports)
WOUND ( 9 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 9 FDA reports)
WRIST FRACTURE ( 9 FDA reports)
ACANTHOSIS NIGRICANS ( 8 FDA reports)
ANKLE FRACTURE ( 8 FDA reports)
ANTICHOLINERGIC SYNDROME ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BEDRIDDEN ( 8 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 8 FDA reports)
BLEPHARITIS ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM DECREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BLOOD URINE ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
BREAST CANCER ( 8 FDA reports)
BREAST HYPERPLASIA ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CELL DEATH ( 8 FDA reports)
CRANIOSYNOSTOSIS ( 8 FDA reports)
DAYDREAMING ( 8 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 8 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 8 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 8 FDA reports)
EMPYEMA ( 8 FDA reports)
GASTRIC POLYPS ( 8 FDA reports)
GASTROINTESTINAL NECROSIS ( 8 FDA reports)
GENERALISED ANXIETY DISORDER ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HAEMORRHAGIC DIATHESIS ( 8 FDA reports)
HEART INJURY ( 8 FDA reports)
HEMIPLEGIA ( 8 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
HERPES VIRUS INFECTION ( 8 FDA reports)
HICCUPS ( 8 FDA reports)
HIP FRACTURE ( 8 FDA reports)
HYPERTHYROIDISM ( 8 FDA reports)
HYPOMAGNESAEMIA ( 8 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 8 FDA reports)
INGUINAL HERNIA ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 8 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 8 FDA reports)
LIGAMENT SPRAIN ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
LIVER TRANSPLANT ( 8 FDA reports)
LYMPHADENECTOMY ( 8 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 8 FDA reports)
MENORRHAGIA ( 8 FDA reports)
MOOD SWINGS ( 8 FDA reports)
MULTIPLE SCLEROSIS ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
NO ADVERSE EVENT ( 8 FDA reports)
NON-CARDIAC CHEST PAIN ( 8 FDA reports)
NYSTAGMUS ( 8 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 8 FDA reports)
ORGANISING PNEUMONIA ( 8 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 8 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 8 FDA reports)
OTITIS EXTERNA ( 8 FDA reports)
OTORRHOEA ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PERSONALITY CHANGE ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
PNEUMONIA LEGIONELLA ( 8 FDA reports)
POLYP ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 8 FDA reports)
PSYCHIATRIC SYMPTOM ( 8 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 8 FDA reports)
RESORPTION BONE INCREASED ( 8 FDA reports)
ROSACEA ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
SKIN FISSURES ( 8 FDA reports)
SKIN ODOUR ABNORMAL ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
THROMBOSIS IN DEVICE ( 8 FDA reports)
THYROID CYST ( 8 FDA reports)
THYROID NEOPLASM ( 8 FDA reports)
TONGUE DISORDER ( 8 FDA reports)
TRISMUS ( 8 FDA reports)
UPPER LIMB FRACTURE ( 8 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 8 FDA reports)
VARICOSE VEIN ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
VISUAL DISTURBANCE ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
ABDOMINAL SYMPTOM ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
AFFECTIVE DISORDER ( 7 FDA reports)
AKATHISIA ( 7 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 7 FDA reports)
ANAEMIA MACROCYTIC ( 7 FDA reports)
APHTHOUS STOMATITIS ( 7 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
BILIARY ANASTOMOSIS ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BRADYCARDIA NEONATAL ( 7 FDA reports)
CENTRAL LINE INFECTION ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CONVULSION NEONATAL ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
COSTOCHONDRITIS ( 7 FDA reports)
DERMATITIS PSORIASIFORM ( 7 FDA reports)
DIABETIC COMPLICATION ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DIAPHRAGMATIC HERNIA ( 7 FDA reports)
DILATATION ATRIAL ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DRUG TOLERANCE ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
ENTEROCOLITIS BACTERIAL ( 7 FDA reports)
ERYTHROSIS ( 7 FDA reports)
EUPHORIC MOOD ( 7 FDA reports)
EXCESSIVE EYE BLINKING ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
EXTRASYSTOLES ( 7 FDA reports)
FIXED ERUPTION ( 7 FDA reports)
FOOD ALLERGY ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
GOITRE ( 7 FDA reports)
GRANULOCYTOPENIA ( 7 FDA reports)
GROWTH RETARDATION ( 7 FDA reports)
GYNAECOMASTIA ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HEPATITIS B ( 7 FDA reports)
HEREDITARY ANGIOEDEMA ( 7 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERMETROPIA ( 7 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 7 FDA reports)
HYPERTENSIVE CRISIS ( 7 FDA reports)
HYPERTONIA NEONATAL ( 7 FDA reports)
HYPOPROTEINAEMIA ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
IMMUNE SYSTEM DISORDER ( 7 FDA reports)
INJECTION SITE PRURITUS ( 7 FDA reports)
INTESTINAL ISCHAEMIA ( 7 FDA reports)
JOINT STABILISATION ( 7 FDA reports)
LABORATORY TEST ABNORMAL ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
LIP EROSION ( 7 FDA reports)
LIVEDO RETICULARIS ( 7 FDA reports)
LYMPHOCYTOSIS ( 7 FDA reports)
MASTECTOMY ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
MIGRAINE WITH AURA ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
NEPHRITIS INTERSTITIAL ( 7 FDA reports)
NEPHROPATHY TOXIC ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
NEUROGENIC BLADDER ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PATHOGEN RESISTANCE ( 7 FDA reports)
PELVIC VENOUS THROMBOSIS ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 7 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 7 FDA reports)
PSEUDOLYMPHOMA ( 7 FDA reports)
PSYCHOMOTOR RETARDATION ( 7 FDA reports)
PUSTULAR PSORIASIS ( 7 FDA reports)
RASH SCARLATINIFORM ( 7 FDA reports)
RENAL ARTERY STENOSIS ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
RETINOPATHY HYPERTENSIVE ( 7 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SACROILIITIS ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SCOLIOSIS ( 7 FDA reports)
SINUS HEADACHE ( 7 FDA reports)
SPINAL COLUMN STENOSIS ( 7 FDA reports)
SPINAL CORPECTOMY ( 7 FDA reports)
SPINAL DECOMPRESSION ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TENSION ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
UROSEPSIS ( 7 FDA reports)
VENTRICULAR FAILURE ( 7 FDA reports)
VENTRICULAR FLUTTER ( 7 FDA reports)
VIRAL PHARYNGITIS ( 7 FDA reports)
VIRAL RASH ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
ACCIDENT ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
AGITATION NEONATAL ( 6 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
AMENORRHOEA ( 6 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
ARTHROSCOPY ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
BRONCHIAL OBSTRUCTION ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
BRONCHOPNEUMOPATHY ( 6 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CEREBRAL DISORDER ( 6 FDA reports)
CLONUS ( 6 FDA reports)
CLUSTER HEADACHE ( 6 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
CONVERSION DISORDER ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DERMATOSIS ( 6 FDA reports)
DRUG PRESCRIBING ERROR ( 6 FDA reports)
DRUG RESISTANCE ( 6 FDA reports)
EAR DISCOMFORT ( 6 FDA reports)
EAR TUBE INSERTION ( 6 FDA reports)
ECZEMA NUMMULAR ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 6 FDA reports)
ENDOCRINE NEOPLASM MALIGNANT ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
EROSIVE DUODENITIS ( 6 FDA reports)
ERYTHRODERMIC PSORIASIS ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYE LASER SURGERY ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
EYELID MARGIN CRUSTING ( 6 FDA reports)
FACIAL BONES FRACTURE ( 6 FDA reports)
FEMORAL NECK FRACTURE ( 6 FDA reports)
FOETAL GROWTH RESTRICTION ( 6 FDA reports)
GAZE PALSY ( 6 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 6 FDA reports)
GLOSSOPTOSIS ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HAEMANGIOMA OF LIVER ( 6 FDA reports)
HOMICIDAL IDEATION ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
INJECTION SITE OEDEMA ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
JUGULAR VEIN DISTENSION ( 6 FDA reports)
KAPOSI'S SARCOMA ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LONG QT SYNDROME ( 6 FDA reports)
LUNG CONSOLIDATION ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MUCOSAL HAEMORRHAGE ( 6 FDA reports)
MYELOFIBROSIS ( 6 FDA reports)
MYOCARDITIS ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NECK INJURY ( 6 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
NODULE ( 6 FDA reports)
OPEN FRACTURE ( 6 FDA reports)
OPPORTUNISTIC INFECTION ( 6 FDA reports)
ORTHOPNOEA ( 6 FDA reports)
PANIC DISORDER ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PERSECUTORY DELUSION ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PLACENTAL INSUFFICIENCY ( 6 FDA reports)
PLASMACYTOMA ( 6 FDA reports)
POLYHYDRAMNIOS ( 6 FDA reports)
RADIAL NERVE PALSY ( 6 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RETINAL ARTERY OCCLUSION ( 6 FDA reports)
SELF ESTEEM DECREASED ( 6 FDA reports)
SICCA SYNDROME ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
STENT PLACEMENT ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
THERAPEUTIC EMBOLISATION ( 6 FDA reports)
THREATENED LABOUR ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
TONGUE BITING ( 6 FDA reports)
TOXOPLASMOSIS ( 6 FDA reports)
TROPONIN T INCREASED ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 6 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
WOUND SECRETION ( 6 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ACCIDENT AT HOME ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANAL ULCER ( 5 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 5 FDA reports)
AORTIC DISSECTION ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BLEPHAROSPASM ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 5 FDA reports)
BLOOD GASES ABNORMAL ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
CARDIAC DEATH ( 5 FDA reports)
CHEYNE-STOKES RESPIRATION ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
COMA SCALE ABNORMAL ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
CYTOGENETIC ABNORMALITY ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
EPIGLOTTIC OEDEMA ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
ESSENTIAL TREMOR ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FOETAL HEART RATE DISORDER ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
GUN SHOT WOUND ( 5 FDA reports)
HAIRY CELL LEUKAEMIA ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HEPATIC TRAUMA ( 5 FDA reports)
HEPATIC VEIN OCCLUSION ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HILAR LYMPHADENOPATHY ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HIP SURGERY ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HOSTILITY ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
INJECTION SITE SWELLING ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
JOINT EFFUSION ( 5 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 5 FDA reports)
LARYNGEAL DYSPNOEA ( 5 FDA reports)
LEG AMPUTATION ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LIVIDITY ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MENSTRUATION IRREGULAR ( 5 FDA reports)
METASTASIS ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MUCOCUTANEOUS RASH ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NODAL RHYTHM ( 5 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 5 FDA reports)
OCCULT BLOOD ( 5 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 5 FDA reports)
OESOPHAGEAL CARCINOMA ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
OPEN WOUND ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
OVARIAN CANCER RECURRENT ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PAPILLOEDEMA ( 5 FDA reports)
PAPULE ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
PERSONALITY DISORDER ( 5 FDA reports)
PHARYNGEAL ERYTHEMA ( 5 FDA reports)
PLEURISY ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
POOR SUCKING REFLEX ( 5 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 5 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
SCAB ( 5 FDA reports)
SCHIZOPHRENIA ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SINUS CONGESTION ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SOMNOLENCE NEONATAL ( 5 FDA reports)
SOPOR ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPINAL FRACTURE ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
TEETH BRITTLE ( 5 FDA reports)
THEFT ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
TINEA VERSICOLOUR ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VENOUS THROMBOSIS LIMB ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
X-RAY ABNORMAL ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
ZINC DEFICIENCY ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ALDOLASE INCREASED ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ANTEROGRADE AMNESIA ( 4 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 4 FDA reports)
BACTERIURIA ( 4 FDA reports)
BALANOPOSTHITIS ( 4 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLAST CELLS ABSENT ( 4 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 4 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE FRAGMENTATION ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BRAIN CONTUSION ( 4 FDA reports)
BREAST CANCER STAGE II ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLANGITIS ACUTE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COGWHEEL RIGIDITY ( 4 FDA reports)
COMPARTMENT SYNDROME ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 4 FDA reports)
CRANIOCEREBRAL INJURY ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
CYANOSIS NEONATAL ( 4 FDA reports)
DEATH NEONATAL ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DIABETIC FOOT ( 4 FDA reports)
DISORDER OF ORBIT ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 4 FDA reports)
DYSHIDROSIS ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
EJECTION FRACTION ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
ESCHERICHIA BACTERAEMIA ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEBRILE CONVULSION ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FINGER DEFORMITY ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GENE MUTATION IDENTIFICATION TEST ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HAND AMPUTATION ( 4 FDA reports)
HAPTOGLOBIN DECREASED ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HIGH ARCHED PALATE ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERVIGILANCE ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE ANAESTHESIA ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INTERTRIGO ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
METASTASES TO MENINGES ( 4 FDA reports)
MONONEUROPATHY ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MYELOCYTOSIS ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
MYOGLOBINAEMIA ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OMPHALITIS ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PALATAL OEDEMA ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
POLYP COLORECTAL ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POST PROCEDURAL CELLULITIS ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RETROGNATHIA ( 4 FDA reports)
RHEUMATOID VASCULITIS ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SCAR EXCISION ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SCRATCH ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SOCIAL PHOBIA ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STOMATITIS NECROTISING ( 4 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 4 FDA reports)
SYSTOLIC HYPERTENSION ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TENSION HEADACHE ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TONGUE EXFOLIATION ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TRACHEAL HAEMORRHAGE ( 4 FDA reports)
TRACHEAL OEDEMA ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TRISOMY 21 ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
UMBILICAL CORD ABNORMALITY ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINE OSMOLARITY INCREASED ( 4 FDA reports)
URTICARIA PAPULAR ( 4 FDA reports)
VAGINAL CYST ( 4 FDA reports)
VAGINAL LESION ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VISCERAL OEDEMA ( 4 FDA reports)
VITAMIN C DEFICIENCY ( 4 FDA reports)
VITAMIN K DECREASED ( 4 FDA reports)
VULVAL CANCER ( 4 FDA reports)
VULVITIS ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WOUND HAEMORRHAGE ( 4 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ABSCESS MANAGEMENT ( 3 FDA reports)
ABULIA ( 3 FDA reports)
ACCOMMODATION DISORDER ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACTIVATION SYNDROME ( 3 FDA reports)
ADENOVIRUS INFECTION ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ALLERGIC HEPATITIS ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
AMINO ACID LEVEL INCREASED ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAEMIA NEONATAL ( 3 FDA reports)
ANAESTHESIA DOLOROSA ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAL INFLAMMATION ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANOREXIA NERVOSA ( 3 FDA reports)
ANOSOGNOSIA ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASTROCYTOMA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTEROIDES INFECTION ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENIGN EAR NEOPLASM ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLADDER DISTENSION ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CAROTID PULSE ABNORMAL ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLEFT LIP AND PALATE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLON POLYPECTOMY ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 3 FDA reports)
COMPULSIONS ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONGENITAL TONGUE ANOMALY ( 3 FDA reports)
CONJUNCTIVAL DISORDER ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CONNECTIVE TISSUE DISORDER ( 3 FDA reports)
CONTRAST MEDIA ALLERGY ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DIABETIC GASTROENTEROPATHY ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISSOCIATIVE DISORDER ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DUODENAL NEOPLASM ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYELID PAIN ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FOETAL CARDIAC DISORDER ( 3 FDA reports)
FOETAL DEATH ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTROENTERITIS BACILLUS ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GENITAL ERYTHEMA ( 3 FDA reports)
GENITAL SWELLING ( 3 FDA reports)
GINGIVAL EROSION ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRIMACING ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMATOMA INFECTION ( 3 FDA reports)
HAEMOGLOBINAEMIA ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
HIP DYSPLASIA ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOSPADIAS ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
JUVENILE ARTHRITIS ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MECONIUM ILEUS ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MENINGORRHAGIA ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MICROLITHIASIS ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORAL MUCOSAL DISORDER ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANCREATIC ISLETS HYPERPLASIA ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERIANAL ERYTHEMA ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERINEAL PAIN ( 3 FDA reports)
PERIORBITAL DISORDER ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PERTUSSIS ( 3 FDA reports)
PHLEBOTOMY ( 3 FDA reports)
PHOSPHENES ( 3 FDA reports)
PIERRE ROBIN SYNDROME ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMATOSIS ( 3 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
POST PROCEDURAL FISTULA ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PROLONGED EXPIRATION ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROSTRATION ( 3 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RED BLOOD CELL ABNORMALITY ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL GRAFT LOSS ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RETROPLACENTAL HAEMATOMA ( 3 FDA reports)
RHABDOMYOSARCOMA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPERINFECTION LUNG ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TRACHEOBRONCHITIS ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
VALVULOPLASTY CARDIAC ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
VIRAEMIA ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE CHEST SYNDROME ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AGONAL DEATH STRUGGLE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANOTIA ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION BIOPSY ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 2 FDA reports)
BETA 2 MICROGLOBULIN DECREASED ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY DRAINAGE ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY LUNG ( 2 FDA reports)
BIOPSY LYMPH GLAND ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN STEM THROMBOSIS ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 2 FDA reports)
CALCIFICATION OF MUSCLE ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CAMPTODACTYLY CONGENITAL ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOMYOPATHY ACUTE ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CHRONIC TONSILLITIS ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLINODACTYLY ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COAGULATION TIME SHORTENED ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CONGENITAL EYELID MALFORMATION ( 2 FDA reports)
CONGENITAL RENAL DISORDER ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL EXFOLIATION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
CYSTITIS VIRAL ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
ECTROPION ( 2 FDA reports)
ECZEMA WEEPING ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
EROSIVE BALANITIS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHROBLASTOSIS ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC FISTULA ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC STENOSIS ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GLARE ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOGLOBIN S DECREASED ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HALLUCINATION, SYNAESTHETIC ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIV TEST POSITIVE ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTERCEPTED MEDICATION ERROR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGITIS VIRAL ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKODYSTROPHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MASSAGE ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MECHANICAL ILEUS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MECONIUM PLUG SYNDROME ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
METABOLIC MYOPATHY ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MICROGNATHIA ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MUCOCUTANEOUS ULCERATION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEONATAL APNOEIC ATTACK ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE SIZE REDUCED ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PITYRIASIS RUBRA PILARIS ( 2 FDA reports)
PLACENTAL INFARCTION ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PNEUMONITIS CHEMICAL ( 2 FDA reports)
PO2 ABNORMAL ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
POLYMERASE CHAIN REACTION ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
RADIATION NECROSIS ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETICULIN INCREASED ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN TEST ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMALL INTESTINAL RESECTION ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STAB WOUND ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TESTICULAR ABSCESS ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
UTERINE ATONY ( 2 FDA reports)
UTERINE DILATION AND EVACUATION ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
UTERINE HYPERTONUS ( 2 FDA reports)
UTERINE HYPOTONUS ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL SKIN INFECTION ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL HAEMATOMA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALDOLASE DECREASED ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALOPECIA SCARRING ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC CAVITY DISORDER ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASSISTED DELIVERY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AUTOTRANSFUSION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE CYST EXCISION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS CHEMICAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOMYOPATHY NEONATAL ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEMENTOPLASTY ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVICAL STRICTURE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLD EXPOSURE INJURY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 1 FDA reports)
CONGENITAL INTESTINAL MALFORMATION ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONGENITAL PYELOCALIECTASIS ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYCLIC NEUTROPENIA ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALOCELE ( 1 FDA reports)
ENDOCRINE NEOPLASM ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROSTOMY CLOSURE ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALSE LABOUR ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PRURITUS MALE ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLUTATHIONE S-TRANSFERASE INCREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATITIS B ANTIBODY ABNORMAL ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERKALIURIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LONG QT SYNDROME CONGENITAL ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MALE REPRODUCTIVE TRACT NEOPLASM ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MAXILLOFACIAL OPERATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS HERPES ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOTIC ALLERGY ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL OVERSEDATION ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NOSOPHOBIA ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTETRICAL PULMONARY EMBOLISM ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALMAR FASCIITIS ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL CANDIDIASIS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYLORUS DILATATION ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIATION EXPOSURE DURING PREGNANCY ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL MYELOGRAM ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOSTOSIS ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRIGONITIS ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URTICARIA CHOLINERGIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR COMPRESSION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN C DECREASED ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WILLIAMS SYNDROME ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use