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

CD4 LYMPHOCYTES DECREASED ( 318 FDA reports)
DRUG INEFFECTIVE ( 287 FDA reports)
PSORIASIS ( 283 FDA reports)
DEATH ( 75 FDA reports)
PYREXIA ( 69 FDA reports)
NAUSEA ( 68 FDA reports)
CONDITION AGGRAVATED ( 63 FDA reports)
FATIGUE ( 61 FDA reports)
PRURITUS ( 60 FDA reports)
HEADACHE ( 55 FDA reports)
DIARRHOEA ( 54 FDA reports)
PNEUMONIA ( 54 FDA reports)
CELLULITIS ( 53 FDA reports)
DIZZINESS ( 50 FDA reports)
NASOPHARYNGITIS ( 50 FDA reports)
CHILLS ( 49 FDA reports)
CEREBROVASCULAR ACCIDENT ( 45 FDA reports)
MYOCARDIAL INFARCTION ( 44 FDA reports)
INFLUENZA LIKE ILLNESS ( 41 FDA reports)
MALAISE ( 41 FDA reports)
ANAEMIA ( 39 FDA reports)
ASTHENIA ( 38 FDA reports)
OFF LABEL USE ( 38 FDA reports)
CHEST PAIN ( 36 FDA reports)
OEDEMA PERIPHERAL ( 36 FDA reports)
DIABETES MELLITUS ( 35 FDA reports)
DYSPNOEA ( 35 FDA reports)
ARTHRALGIA ( 34 FDA reports)
COUGH ( 32 FDA reports)
URINARY TRACT INFECTION ( 32 FDA reports)
VOMITING ( 32 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 31 FDA reports)
PAIN ( 31 FDA reports)
DEHYDRATION ( 30 FDA reports)
MYALGIA ( 30 FDA reports)
HYPOTENSION ( 29 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 29 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 28 FDA reports)
FALL ( 28 FDA reports)
HERPES ZOSTER ( 28 FDA reports)
SINUSITIS ( 28 FDA reports)
STAPHYLOCOCCAL INFECTION ( 28 FDA reports)
BLOOD GLUCOSE INCREASED ( 27 FDA reports)
CORONARY ARTERY DISEASE ( 27 FDA reports)
PLATELET COUNT DECREASED ( 27 FDA reports)
RENAL FAILURE ( 27 FDA reports)
RESPIRATORY FAILURE ( 27 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 26 FDA reports)
HYPERTENSION ( 25 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 24 FDA reports)
SEPSIS ( 24 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 23 FDA reports)
SURGERY ( 23 FDA reports)
BRONCHITIS ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
LYMPHADENOPATHY ( 22 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 22 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
ABDOMINAL PAIN ( 20 FDA reports)
ATRIAL FIBRILLATION ( 20 FDA reports)
INFLUENZA ( 20 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
INJECTION SITE PAIN ( 18 FDA reports)
VIRAL INFECTION ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
ASTHMA ( 17 FDA reports)
CD4 LYMPHOCYTES ( 17 FDA reports)
URTICARIA ( 17 FDA reports)
ANXIETY ( 16 FDA reports)
BACK PAIN ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
DERMATITIS EXFOLIATIVE ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 16 FDA reports)
ARTHRITIS ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
CARDIO-RESPIRATORY ARREST ( 15 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 15 FDA reports)
DEPRESSION ( 15 FDA reports)
DIVERTICULITIS ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
LABORATORY TEST ABNORMAL ( 15 FDA reports)
LIVER DISORDER ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
NEPHROLITHIASIS ( 15 FDA reports)
PSORIATIC ARTHROPATHY ( 15 FDA reports)
RENAL DISORDER ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
ERYTHEMA ( 14 FDA reports)
HAEMATOCRIT DECREASED ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
ATELECTASIS ( 13 FDA reports)
CARDIAC DISORDER ( 13 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 13 FDA reports)
NEUTROPENIA ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
PARAESTHESIA ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
ANGINA PECTORIS ( 12 FDA reports)
ANTIBODY TEST POSITIVE ( 12 FDA reports)
COAGULOPATHY ( 12 FDA reports)
LUNG NEOPLASM MALIGNANT ( 12 FDA reports)
MENTAL STATUS CHANGES ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
RASH ( 12 FDA reports)
ROAD TRAFFIC ACCIDENT ( 12 FDA reports)
ABORTION SPONTANEOUS ( 11 FDA reports)
APPENDICITIS ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BLOOD ALBUMIN DECREASED ( 11 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
INFECTION ( 11 FDA reports)
PANCREATITIS ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
POST PROCEDURAL COMPLICATION ( 11 FDA reports)
SEPTIC SHOCK ( 11 FDA reports)
SKIN BURNING SENSATION ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 10 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
DISEASE RECURRENCE ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 10 FDA reports)
JOINT SWELLING ( 10 FDA reports)
MYCOSIS FUNGOIDES ( 10 FDA reports)
NO THERAPEUTIC RESPONSE ( 10 FDA reports)
PROSTATE CANCER ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
RASH MACULAR ( 10 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
BASAL CELL CARCINOMA ( 9 FDA reports)
BLADDER CANCER ( 9 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BONE PAIN ( 9 FDA reports)
CAESAREAN SECTION ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
GASTRITIS ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
IMMUNOSUPPRESSION ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
POSTOPERATIVE INFECTION ( 9 FDA reports)
PREGNANCY ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 9 FDA reports)
STRESS ( 9 FDA reports)
SWELLING ( 9 FDA reports)
T-CELL LYMPHOMA ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
ARTHRITIS INFECTIVE ( 8 FDA reports)
B-CELL LYMPHOMA STAGE I ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
HOSPITALISATION ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
THERAPY NON-RESPONDER ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
ALOPECIA ( 7 FDA reports)
ANGINA UNSTABLE ( 7 FDA reports)
BILE DUCT STONE ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
FURUNCLE ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
INFLAMMATION ( 7 FDA reports)
INJECTION SITE BURNING ( 7 FDA reports)
INJURY ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
LYMPHOMA ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PUSTULAR PSORIASIS ( 7 FDA reports)
RASH PRURITIC ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
CD4/CD8 RATIO INCREASED ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
FAILURE TO THRIVE ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
GASTROENTERITIS RADIATION ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMOGLOBIN INCREASED ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
MENINGITIS VIRAL ( 6 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ABDOMINAL HERNIA ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ANEURYSM ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CYSTITIS ESCHERICHIA ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DIFFICULTY IN WALKING ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC VARICES ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
GOUT ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
OBESITY ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PRE-ECLAMPSIA ( 5 FDA reports)
PROSTATITIS ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
SCAB ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ADENOMYOSIS ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
GRANULOMA ANNULARE ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MASS ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SCAR ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SENSATION OF HEAVINESS ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN INFECTION ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
STRESS SYMPTOMS ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
URETERIC OBSTRUCTION ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABORTION ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASPERGILLOMA ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD IRON INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLON CANCER STAGE III ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPIDERMAL NAEVUS ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
EXTERNAL EAR CELLULITIS ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEAR ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAND AMPUTATION ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MENOMETRORRHAGIA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PIGMENTED NAEVUS ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
RASH SCALY ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINITIS GARDNERELLA ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLADDER CANCER STAGE IV ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRONCHIAL CYST ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CD8 LYMPHOCYTES ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COMA ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECTROPION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LIPASE DECREASED ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL FLARING ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NODULE ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN BLEEDING ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
UNWANTED PREGNANCY ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX CARCINOMA STAGE I ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD EXPOSURE INJURY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIDIDYMAL CYST ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE II ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRACTURED ZYGOMATIC ARCH ELEVATION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NASAL VESTIBULITIS ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
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OBESITY SURGERY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVARIAN ADHESION ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARACENTESIS ABDOMEN ABNORMAL ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
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PERITONSILLAR ABSCESS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
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PHOTOSENSITIVE RASH ( 1 FDA reports)
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PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
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POLYP ( 1 FDA reports)
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POST PROCEDURAL FISTULA ( 1 FDA reports)
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POSTOPERATIVE FEVER ( 1 FDA reports)
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PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
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PROSTATIC DISORDER ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
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RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
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SARCOMA UTERUS ( 1 FDA reports)
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SEBORRHOEIC KERATOSIS ( 1 FDA reports)
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SERUM FERRITIN DECREASED ( 1 FDA reports)
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SERUM SICKNESS ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
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SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
T-LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TANNING ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR GERM CELL CANCER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THORACIC OPERATION ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TONSILLAR CYST ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENIPUNCTURE SITE REACTION ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
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X-RAY ABNORMAL ( 1 FDA reports)

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