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

PYREXIA ( 116 FDA reports)
PAIN ( 95 FDA reports)
ANXIETY ( 81 FDA reports)
DYSPNOEA ( 79 FDA reports)
PNEUMONIA ( 78 FDA reports)
ANAEMIA ( 68 FDA reports)
NAUSEA ( 65 FDA reports)
DIARRHOEA ( 64 FDA reports)
OSTEONECROSIS OF JAW ( 63 FDA reports)
NEUTROPENIA ( 62 FDA reports)
FATIGUE ( 60 FDA reports)
VOMITING ( 58 FDA reports)
DRUG INEFFECTIVE ( 57 FDA reports)
THROMBOCYTOPENIA ( 57 FDA reports)
RASH ( 55 FDA reports)
INJURY ( 54 FDA reports)
RENAL FAILURE ACUTE ( 54 FDA reports)
ARTHRALGIA ( 52 FDA reports)
HERPES ZOSTER ( 51 FDA reports)
BACK PAIN ( 48 FDA reports)
HEADACHE ( 48 FDA reports)
MUCOSAL INFLAMMATION ( 46 FDA reports)
ASTHENIA ( 45 FDA reports)
PANCYTOPENIA ( 44 FDA reports)
FEBRILE NEUTROPENIA ( 42 FDA reports)
PLATELET COUNT DECREASED ( 40 FDA reports)
TOOTH EXTRACTION ( 40 FDA reports)
HYPOTENSION ( 39 FDA reports)
MULTIPLE MYELOMA ( 38 FDA reports)
PLEURAL EFFUSION ( 38 FDA reports)
ABDOMINAL PAIN ( 37 FDA reports)
DEPRESSION ( 37 FDA reports)
NEUROPATHY PERIPHERAL ( 36 FDA reports)
SEPSIS ( 36 FDA reports)
COUGH ( 35 FDA reports)
DIZZINESS ( 35 FDA reports)
INFECTION ( 35 FDA reports)
CONSTIPATION ( 34 FDA reports)
DEHYDRATION ( 34 FDA reports)
HAEMOGLOBIN DECREASED ( 34 FDA reports)
PAIN IN EXTREMITY ( 34 FDA reports)
RENAL FAILURE ( 34 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 34 FDA reports)
BLOOD CREATININE INCREASED ( 33 FDA reports)
OEDEMA PERIPHERAL ( 33 FDA reports)
BONE PAIN ( 32 FDA reports)
RESPIRATORY FAILURE ( 32 FDA reports)
STEM CELL TRANSPLANT ( 32 FDA reports)
FALL ( 31 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 31 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 31 FDA reports)
URINARY TRACT INFECTION ( 31 FDA reports)
MALAISE ( 30 FDA reports)
MUSCULAR WEAKNESS ( 29 FDA reports)
OSTEOARTHRITIS ( 29 FDA reports)
ANHEDONIA ( 28 FDA reports)
ATELECTASIS ( 28 FDA reports)
CHILLS ( 28 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 28 FDA reports)
DECREASED APPETITE ( 28 FDA reports)
SINUSITIS ( 28 FDA reports)
CHEST PAIN ( 27 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 27 FDA reports)
DEATH ( 27 FDA reports)
HYPERTENSION ( 27 FDA reports)
HYPOAESTHESIA ( 27 FDA reports)
IMPAIRED HEALING ( 27 FDA reports)
PAIN IN JAW ( 27 FDA reports)
TREMOR ( 27 FDA reports)
DYSPHAGIA ( 26 FDA reports)
EMOTIONAL DISTRESS ( 26 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 26 FDA reports)
MYALGIA ( 26 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
BONE DISORDER ( 24 FDA reports)
OSTEOMYELITIS ( 24 FDA reports)
PRURITUS ( 24 FDA reports)
SPINAL OSTEOARTHRITIS ( 24 FDA reports)
ABDOMINAL PAIN UPPER ( 23 FDA reports)
CONVULSION ( 23 FDA reports)
HYPOKALAEMIA ( 23 FDA reports)
INSOMNIA ( 23 FDA reports)
MULTI-ORGAN FAILURE ( 23 FDA reports)
WEIGHT DECREASED ( 23 FDA reports)
DEEP VEIN THROMBOSIS ( 22 FDA reports)
PARAESTHESIA ( 22 FDA reports)
ATRIAL FIBRILLATION ( 21 FDA reports)
DRUG INTERACTION ( 21 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 21 FDA reports)
OSTEOPENIA ( 21 FDA reports)
STAPHYLOCOCCAL INFECTION ( 21 FDA reports)
STOMATITIS ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 20 FDA reports)
SINUS TACHYCARDIA ( 20 FDA reports)
SWELLING ( 20 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
BONE LESION ( 19 FDA reports)
DECREASED INTEREST ( 19 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
OSTEOPOROSIS ( 19 FDA reports)
BLISTER ( 18 FDA reports)
BRONCHITIS ( 18 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 18 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 18 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 18 FDA reports)
HAEMATOCRIT DECREASED ( 18 FDA reports)
HYPERGLYCAEMIA ( 18 FDA reports)
HYPOTHYROIDISM ( 18 FDA reports)
MUSCLE SPASMS ( 18 FDA reports)
RECTAL HAEMORRHAGE ( 18 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 18 FDA reports)
BLOOD BILIRUBIN INCREASED ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
DISABILITY ( 17 FDA reports)
DISCOMFORT ( 17 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 17 FDA reports)
GINGIVAL INFECTION ( 17 FDA reports)
HEPATOTOXICITY ( 17 FDA reports)
HYPERCALCAEMIA ( 17 FDA reports)
HYPONATRAEMIA ( 17 FDA reports)
HYPOXIA ( 17 FDA reports)
ARTHROPATHY ( 16 FDA reports)
CELLULITIS ( 16 FDA reports)
DEFORMITY ( 16 FDA reports)
OSTEONECROSIS ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
DYSPEPSIA ( 15 FDA reports)
GAIT DISTURBANCE ( 15 FDA reports)
GRAFT VERSUS HOST DISEASE ( 15 FDA reports)
HEPATIC ENZYME INCREASED ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
LUNG INFILTRATION ( 15 FDA reports)
LYMPHADENOPATHY ( 15 FDA reports)
MENTAL STATUS CHANGES ( 15 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 15 FDA reports)
OEDEMA ( 15 FDA reports)
RENAL IMPAIRMENT ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
METASTASES TO BONE ( 14 FDA reports)
NEUTROPENIC SEPSIS ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
RENAL FAILURE CHRONIC ( 14 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
BACTERAEMIA ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
COMPRESSION FRACTURE ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
DIABETES MELLITUS ( 13 FDA reports)
DYSURIA ( 13 FDA reports)
ORAL DISORDER ( 13 FDA reports)
ORAL PAIN ( 13 FDA reports)
OROPHARYNGEAL PAIN ( 13 FDA reports)
OSTEOLYSIS ( 13 FDA reports)
SPINAL COMPRESSION FRACTURE ( 13 FDA reports)
UNRESPONSIVE TO STIMULI ( 13 FDA reports)
AGITATION ( 12 FDA reports)
CEREBRAL INFARCTION ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
HAEMATOCHEZIA ( 12 FDA reports)
HAEMATOTOXICITY ( 12 FDA reports)
LEUKOPENIA ( 12 FDA reports)
LIFE EXPECTANCY SHORTENED ( 12 FDA reports)
LIVER DISORDER ( 12 FDA reports)
LUNG NEOPLASM ( 12 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
RASH PRURITIC ( 12 FDA reports)
SPINAL DISORDER ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
ABDOMINAL DISCOMFORT ( 11 FDA reports)
ASCITES ( 11 FDA reports)
AZOTAEMIA ( 11 FDA reports)
BONE MARROW TRANSPLANT ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
FLUID OVERLOAD ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HAEMORRHOIDS ( 11 FDA reports)
HERPES VIRUS INFECTION ( 11 FDA reports)
HYPOGLYCAEMIA ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
MELAENA ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
PRODUCTIVE COUGH ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 11 FDA reports)
RENAL CYST ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
ARTHRITIS ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
DYSPHEMIA ( 10 FDA reports)
DYSPNOEA EXERTIONAL ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
GASTRITIS ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
GINGIVAL RECESSION ( 10 FDA reports)
GINGIVAL SWELLING ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HALLUCINATION ( 10 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
HIATUS HERNIA ( 10 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
JOINT SWELLING ( 10 FDA reports)
LETHARGY ( 10 FDA reports)
LYMPHOPENIA ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
NIGHT SWEATS ( 10 FDA reports)
ORAL HERPES ( 10 FDA reports)
RIB FRACTURE ( 10 FDA reports)
SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
STRESS ( 10 FDA reports)
SURGERY ( 10 FDA reports)
TOOTH ABSCESS ( 10 FDA reports)
TRANSAMINASES INCREASED ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
ABDOMINAL PAIN LOWER ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
ADRENAL INSUFFICIENCY ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BONE GRAFT ( 9 FDA reports)
DECUBITUS ULCER ( 9 FDA reports)
DENTURE WEARER ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
DRUG TOXICITY ( 9 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
JAW OPERATION ( 9 FDA reports)
LOOSE TOOTH ( 9 FDA reports)
MALNUTRITION ( 9 FDA reports)
MUSCLE TIGHTNESS ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
RASH ERYTHEMATOUS ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
SYNOVIAL CYST ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ACTINIC KERATOSIS ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BONE DEBRIDEMENT ( 8 FDA reports)
CANDIDIASIS ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
COLONIC POLYP ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
ENDODONTIC PROCEDURE ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERCOAGULATION ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
MASTOIDITIS ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
NODULE ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PHYSICAL DISABILITY ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
SCIATICA ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
VENOUS INSUFFICIENCY ( 8 FDA reports)
ABASIA ( 7 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BASAL CELL CARCINOMA ( 7 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
BRONCHIECTASIS ( 7 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CATARACT ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DENTAL PROSTHESIS USER ( 7 FDA reports)
DEVICE RELATED INFECTION ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
ENTEROCOCCAL INFECTION ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
FRACTURED SACRUM ( 7 FDA reports)
GINGIVAL DISORDER ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
JAUNDICE ( 7 FDA reports)
JOINT STIFFNESS ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
NEPHROPATHY TOXIC ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
PANCREATIC CARCINOMA ( 7 FDA reports)
PELVIC FRACTURE ( 7 FDA reports)
PLASMACYTOMA ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
ROTATOR CUFF SYNDROME ( 7 FDA reports)
SCAR ( 7 FDA reports)
SINUS CONGESTION ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
ABSCESS DRAINAGE ( 6 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
AMNESIA ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
ASPIRATION ( 6 FDA reports)
ASTIGMATISM ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BONE OPERATION ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
COMA ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FISTULA ( 6 FDA reports)
FOOT FRACTURE ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPOCALCAEMIA ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
LARGE INTESTINE PERFORATION ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
MASS ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
NEPHROLITHIASIS ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SCOLIOSIS ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SMALL INTESTINE CARCINOMA ( 6 FDA reports)
SOFT TISSUE INFLAMMATION ( 6 FDA reports)
SPINAL DEFORMITY ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
THROMBOPHLEBITIS ( 6 FDA reports)
TOOTHACHE ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TRANSPLANT FAILURE ( 6 FDA reports)
VERTEBROPLASTY ( 6 FDA reports)
ACIDOSIS ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BONE SCAN ABNORMAL ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
COLON ADENOMA ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
ESCHERICHIA INFECTION ( 5 FDA reports)
EYE SWELLING ( 5 FDA reports)
FAILURE TO THRIVE ( 5 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
GOITRE ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MASTICATION DISORDER ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
OSTEOMYELITIS ACUTE ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PROSTATOMEGALY ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
STREPTOCOCCAL SEPSIS ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOOTH IMPACTED ( 5 FDA reports)
TUMOUR FLARE ( 5 FDA reports)
VAGINAL INFECTION ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
ANGIOLIPOMA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
BACTERIAL DISEASE CARRIER ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BONE ATROPHY ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
BUNION ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 4 FDA reports)
DENTAL IMPLANTATION ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
GENITAL HERPES ( 4 FDA reports)
GINGIVAL EROSION ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HERPES OPHTHALMIC ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERKERATOSIS ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LIPOMA EXCISION ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
MASS EXCISION ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MERALGIA PARAESTHETICA ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
MYELOMA RECURRENCE ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
PANCREATIC HAEMORRHAGE ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PERIVASCULAR DERMATITIS ( 4 FDA reports)
PHLEBOLITH ( 4 FDA reports)
PITUITARY ENLARGEMENT ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMATOSIS ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POLYARTERITIS NODOSA ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
PRESBYOPIA ( 4 FDA reports)
PROSTATECTOMY ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RADICULOPATHY ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETINOIC ACID SYNDROME ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPLENIC INJURY ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 4 FDA reports)
THROMBOSED VARICOSE VEIN ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
TOOTH FRACTURE ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TOOTH REPAIR ( 4 FDA reports)
TOXOPLASMOSIS ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
VARICOSE VEIN OPERATION ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
VIRAL LABYRINTHITIS ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
AGNOSIA ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BACTERIAL DIARRHOEA ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BIOPSY BONE MARROW ( 3 FDA reports)
BLADDER NECK OPERATION ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE EROSION ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BULIMIA NERVOSA ( 3 FDA reports)
BULLOUS LUNG DISEASE ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLPOCELE ( 3 FDA reports)
CORNEAL OPERATION ( 3 FDA reports)
CUTIS LAXA ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
CYSTOSCOPY ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DERMATOPHYTOSIS ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOSCOPY ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INFECTIVE TENOSYNOVITIS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JARISCH-HERXHEIMER REACTION ( 3 FDA reports)
JEJUNECTOMY ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LYMPHADENECTOMY ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 3 FDA reports)
MEIBOMIANITIS ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NECROTISING RETINITIS ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NERVE ROOT COMPRESSION ( 3 FDA reports)
NERVE ROOT LESION ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUROPATHIC ULCER ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OESOPHAGEAL RUPTURE ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OSTEOMA ( 3 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 3 FDA reports)
PANCREATICODUODENECTOMY ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PINGUECULA ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLASMACYTOSIS ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RETICULOCYTE COUNT INCREASED ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
SPINAL LAMINECTOMY ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
STENT REMOVAL ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VULVITIS ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALVEOLOPLASTY ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE FISTULA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS BACTERIAL ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOREDUCTIVE SURGERY ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LABEL CONFUSION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROBACTER SEPSIS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOLLICULAR MUCINOSIS ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MEDULLOBLASTOMA ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
ORTHOSIS USER ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PLATELET TOXICITY ( 2 FDA reports)
PLEURECTOMY ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SCROTAL IRRITATION ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SHOULDER DEFORMITY ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPINAL CORPECTOMY ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPONDYLITIC MYELOPATHY ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TENDON GRAFT ( 2 FDA reports)
THALASSAEMIA ALPHA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISCERAL OEDEMA ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTINIC ELASTOSIS ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIOPSY GINGIVAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD STEM CELL HARVEST ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE LESION EXCISION ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIURETIC THERAPY ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
DYSPONESIS ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPIGLOTTITIS OBSTRUCTIVE ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FEVER NEONATAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GEOTRICHUM INFECTION ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHERMIA NEONATAL ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTIOUS DISEASE CARRIER ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLUVER-BUCY SYNDROME ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE COUNT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION CRYSTALS IN URINE ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METATARSUS PRIMUS VARUS ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULAR FASCIITIS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FIBROMA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSA ATROPHY ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHODONTIC APPLIANCE USER ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PTERYGIUM ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RADIATION NEUROPATHY ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RICHTER'S SYNDROME ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCLERAL OPERATION ( 1 FDA reports)
SCROTAL CYST ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGOTOMY ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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