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

PAIN ( 84 FDA reports)
BACK PAIN ( 83 FDA reports)
NAUSEA ( 74 FDA reports)
ANAEMIA ( 72 FDA reports)
OSTEONECROSIS OF JAW ( 71 FDA reports)
ANXIETY ( 69 FDA reports)
DYSPNOEA ( 64 FDA reports)
PYREXIA ( 57 FDA reports)
OSTEOMYELITIS ( 55 FDA reports)
INJURY ( 54 FDA reports)
DIARRHOEA ( 50 FDA reports)
PNEUMONIA ( 49 FDA reports)
ABDOMINAL PAIN ( 48 FDA reports)
FATIGUE ( 48 FDA reports)
PLEURAL EFFUSION ( 48 FDA reports)
INFECTION ( 43 FDA reports)
PAIN IN EXTREMITY ( 43 FDA reports)
ARTHRALGIA ( 42 FDA reports)
BONE DISORDER ( 42 FDA reports)
PAIN IN JAW ( 42 FDA reports)
FALL ( 40 FDA reports)
VOMITING ( 40 FDA reports)
HYPERTENSION ( 39 FDA reports)
OSTEOARTHRITIS ( 39 FDA reports)
CONSTIPATION ( 37 FDA reports)
EMOTIONAL DISTRESS ( 36 FDA reports)
ATELECTASIS ( 35 FDA reports)
DEPRESSION ( 35 FDA reports)
HYPOAESTHESIA ( 35 FDA reports)
WEIGHT DECREASED ( 35 FDA reports)
STRESS ( 34 FDA reports)
HYPERHIDROSIS ( 33 FDA reports)
HYPOTENSION ( 33 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
WEIGHT INCREASED ( 33 FDA reports)
OEDEMA PERIPHERAL ( 32 FDA reports)
URINARY TRACT INFECTION ( 32 FDA reports)
SPINAL OSTEOARTHRITIS ( 31 FDA reports)
CHEST PAIN ( 29 FDA reports)
NEUROPATHY PERIPHERAL ( 29 FDA reports)
RASH ( 29 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 28 FDA reports)
PRIMARY SEQUESTRUM ( 28 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 27 FDA reports)
MITRAL VALVE INCOMPETENCE ( 27 FDA reports)
SINUSITIS ( 27 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 26 FDA reports)
DIZZINESS ( 26 FDA reports)
RESPIRATORY FAILURE ( 26 FDA reports)
BLOOD CREATININE INCREASED ( 25 FDA reports)
CONFUSIONAL STATE ( 25 FDA reports)
EXOSTOSIS ( 25 FDA reports)
GAIT DISTURBANCE ( 25 FDA reports)
HEADACHE ( 25 FDA reports)
HYPERLIPIDAEMIA ( 25 FDA reports)
IMPAIRED HEALING ( 25 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 24 FDA reports)
DEHYDRATION ( 24 FDA reports)
HAEMORRHOIDS ( 24 FDA reports)
PULMONARY EMBOLISM ( 24 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 24 FDA reports)
ANHEDONIA ( 23 FDA reports)
ATRIAL FIBRILLATION ( 23 FDA reports)
CARDIOMEGALY ( 23 FDA reports)
DEATH ( 23 FDA reports)
DEEP VEIN THROMBOSIS ( 23 FDA reports)
DYSPHAGIA ( 23 FDA reports)
INSOMNIA ( 23 FDA reports)
LYMPHADENOPATHY ( 23 FDA reports)
SEPSIS ( 23 FDA reports)
ASTHENIA ( 22 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
MASTICATION DISORDER ( 21 FDA reports)
PARAESTHESIA ( 21 FDA reports)
PROTHROMBIN TIME PROLONGED ( 21 FDA reports)
RENAL CYST ( 21 FDA reports)
THROMBOCYTOPENIA ( 21 FDA reports)
TOOTH DISORDER ( 21 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
DECREASED APPETITE ( 20 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 20 FDA reports)
RENAL FAILURE ( 20 FDA reports)
DENTAL CARIES ( 19 FDA reports)
DYSURIA ( 19 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 19 FDA reports)
METASTASES TO BONE ( 19 FDA reports)
NEOPLASM MALIGNANT ( 19 FDA reports)
SPINAL COMPRESSION FRACTURE ( 19 FDA reports)
ARTERIOSCLEROSIS ( 18 FDA reports)
BONE LESION ( 18 FDA reports)
CONVULSION ( 18 FDA reports)
COUGH ( 18 FDA reports)
DEFORMITY ( 18 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 18 FDA reports)
GINGIVITIS ( 18 FDA reports)
HYPERCALCAEMIA ( 18 FDA reports)
LOOSE TOOTH ( 18 FDA reports)
METASTASES TO LUNG ( 18 FDA reports)
PHYSICAL DISABILITY ( 18 FDA reports)
SWELLING FACE ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
VISUAL IMPAIRMENT ( 18 FDA reports)
CATARACT ( 17 FDA reports)
EXPOSED BONE IN JAW ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
MYOCARDIAL INFARCTION ( 17 FDA reports)
BRONCHITIS ( 16 FDA reports)
HIATUS HERNIA ( 16 FDA reports)
MULTI-ORGAN FAILURE ( 16 FDA reports)
SYNCOPE ( 16 FDA reports)
TOOTH LOSS ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
ERECTILE DYSFUNCTION ( 15 FDA reports)
FISTULA ( 15 FDA reports)
FLANK PAIN ( 15 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
HYPOKALAEMIA ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
OSTEOPENIA ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 14 FDA reports)
CHOLELITHIASIS ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
ENTEROCOCCAL INFECTION ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
LIFE EXPECTANCY SHORTENED ( 14 FDA reports)
LUNG NEOPLASM ( 14 FDA reports)
METASTASES TO SPINE ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
PNEUMOTHORAX ( 14 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
SPINAL COLUMN STENOSIS ( 14 FDA reports)
VERTIGO ( 14 FDA reports)
AORTIC ANEURYSM ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
BLOOD URINE PRESENT ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
MUCOSAL INFLAMMATION ( 13 FDA reports)
MUSCLE TWITCHING ( 13 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
NEPHROLITHIASIS ( 13 FDA reports)
OBESITY ( 13 FDA reports)
PELVIC PAIN ( 13 FDA reports)
SLEEP APNOEA SYNDROME ( 13 FDA reports)
TINNITUS ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
BURSITIS ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
CORONARY ARTERY DISEASE ( 12 FDA reports)
GYNAECOMASTIA ( 12 FDA reports)
HYPOPHAGIA ( 12 FDA reports)
IRRITABLE BOWEL SYNDROME ( 12 FDA reports)
LEUKOCYTOSIS ( 12 FDA reports)
ONYCHOMYCOSIS ( 12 FDA reports)
POLLAKIURIA ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
SWELLING ( 12 FDA reports)
TOOTHACHE ( 12 FDA reports)
WHEEZING ( 12 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CHILLS ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
GASTRITIS ( 11 FDA reports)
HYPOACUSIS ( 11 FDA reports)
MITRAL VALVE PROLAPSE ( 11 FDA reports)
NECK PAIN ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
PULPITIS DENTAL ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
RHINITIS ( 11 FDA reports)
TOOTH FRACTURE ( 11 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BONE DEBRIDEMENT ( 10 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 10 FDA reports)
CEREBRAL ISCHAEMIA ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
COLITIS ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
CYST ( 10 FDA reports)
DEAFNESS ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
DIVERTICULUM INTESTINAL ( 10 FDA reports)
EAR PAIN ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
ISCHAEMIA ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MALNUTRITION ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
NEONATAL DISORDER ( 10 FDA reports)
OPEN WOUND ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 10 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 9 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
CARPAL TUNNEL SYNDROME ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
DIVERTICULITIS ( 9 FDA reports)
DIVERTICULUM ( 9 FDA reports)
FEBRILE NEUTROPENIA ( 9 FDA reports)
GINGIVAL DISORDER ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HYDRONEPHROSIS ( 9 FDA reports)
HYPOTHYROIDISM ( 9 FDA reports)
LEFT ATRIAL DILATATION ( 9 FDA reports)
MALIGNANT MELANOMA ( 9 FDA reports)
MENTAL STATUS CHANGES ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
NASAL CONGESTION ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
TOOTH ABSCESS ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ABSCESS ORAL ( 8 FDA reports)
BONE LOSS ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
CAROTID BRUIT ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
COMPRESSION FRACTURE ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
EXCORIATION ( 8 FDA reports)
FEAR ( 8 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 8 FDA reports)
GALLBLADDER DISORDER ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
METASTASES TO ABDOMINAL WALL ( 8 FDA reports)
MUSCULOSKELETAL PAIN ( 8 FDA reports)
NASAL SEPTUM DEVIATION ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
ORAL PAIN ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
OSTEOSCLEROSIS ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
PRESYNCOPE ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RADICULAR CYST ( 8 FDA reports)
RADICULOPATHY ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
SCAR ( 8 FDA reports)
SCIATICA ( 8 FDA reports)
SCOLIOSIS ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 8 FDA reports)
SPLENIC CALCIFICATION ( 8 FDA reports)
TESTICULAR PAIN ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
UNEVALUABLE EVENT ( 8 FDA reports)
WALKING AID USER ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 7 FDA reports)
AMNESIA ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
APPENDICITIS ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CARDIAC VALVE ABSCESS ( 7 FDA reports)
CAROTID ARTERY DISEASE ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
COLON ADENOMA ( 7 FDA reports)
COORDINATION ABNORMAL ( 7 FDA reports)
DERMATITIS ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
EPIDIDYMITIS ( 7 FDA reports)
GINGIVAL ULCERATION ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HYDROCELE ( 7 FDA reports)
HYPERMETABOLISM ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 7 FDA reports)
JOINT EFFUSION ( 7 FDA reports)
LIBIDO DECREASED ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
MULTIPLE MYELOMA ( 7 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 7 FDA reports)
ORAL INFECTION ( 7 FDA reports)
ORCHITIS ( 7 FDA reports)
OSTEOLYSIS ( 7 FDA reports)
PERIPHERAL EMBOLISM ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
PLASMACYTOMA ( 7 FDA reports)
PLEURAL FIBROSIS ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
PULMONARY GRANULOMA ( 7 FDA reports)
PURULENCE ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
RENAL INJURY ( 7 FDA reports)
RENAL ISCHAEMIA ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
STRIDOR ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TESTICULAR SWELLING ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
ADENOIDAL HYPERTROPHY ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ANEURYSM ( 6 FDA reports)
APPENDICITIS PERFORATED ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 6 FDA reports)
AUTISM ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
BREAST PROSTHESIS USER ( 6 FDA reports)
BREATH ODOUR ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DEVICE OCCLUSION ( 6 FDA reports)
DROP ATTACKS ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
FOETAL HEART RATE DECELERATION ( 6 FDA reports)
GOUT ( 6 FDA reports)
HEARING AID USER ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
KYPHOSIS ( 6 FDA reports)
LARYNGEAL STENOSIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LOBAR PNEUMONIA ( 6 FDA reports)
LUMBAR SPINE FLATTENING ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MASS ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
METATARSALGIA ( 6 FDA reports)
MORTON'S NEUROMA ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 6 FDA reports)
NODAL OSTEOARTHRITIS ( 6 FDA reports)
OTITIS MEDIA CHRONIC ( 6 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 6 FDA reports)
PERIARTHRITIS ( 6 FDA reports)
PERIODONTITIS ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
PULMONARY MASS ( 6 FDA reports)
PULMONARY RADIATION INJURY ( 6 FDA reports)
PURULENT DISCHARGE ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
RHONCHI ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
STEM CELL TRANSPLANT ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
THYROID NEOPLASM ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TRISMUS ( 6 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VIRAL PHARYNGITIS ( 6 FDA reports)
ACNE ( 5 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 5 FDA reports)
ACTINOMYCOSIS ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
APGAR SCORE LOW ( 5 FDA reports)
APHAKIA ( 5 FDA reports)
APHONIA ( 5 FDA reports)
ASCITES ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 5 FDA reports)
BLOOD GASES ABNORMAL ( 5 FDA reports)
BONE MARROW OEDEMA ( 5 FDA reports)
CANDIDA SEPSIS ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CEREBRAL PALSY ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CONGENITAL ANOMALY ( 5 FDA reports)
CONGENITAL KNEE DEFORMITY ( 5 FDA reports)
CONGENITAL NYSTAGMUS ( 5 FDA reports)
COOMBS TEST POSITIVE ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DEVICE BREAKAGE ( 5 FDA reports)
DISABLED RELATIVE ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HAEMATOCRIT INCREASED ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 5 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 5 FDA reports)
IRIDOCELE ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 5 FDA reports)
MECONIUM STAIN ( 5 FDA reports)
MENTAL RETARDATION ( 5 FDA reports)
MICTURITION URGENCY ( 5 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
NOCTURIA ( 5 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 5 FDA reports)
OSTEOCHONDROSIS ( 5 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PIGMENTATION DISORDER ( 5 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 5 FDA reports)
PROSTATIC OBSTRUCTION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PULMONARY CALCIFICATION ( 5 FDA reports)
RETINAL DETACHMENT ( 5 FDA reports)
SACCADIC EYE MOVEMENT ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TONGUE DISCOLOURATION ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
UNEQUAL LIMB LENGTH ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BONE SWELLING ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHRONIC TONSILLITIS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 4 FDA reports)
CONJUNCTIVAL ABRASION ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FOETAL DISTRESS SYNDROME ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
GINGIVAL SWELLING ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 4 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 4 FDA reports)
MACULAR SCAR ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
MICROCYTIC ANAEMIA ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PERITONSILLAR ABSCESS ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SENSITIVITY OF TEETH ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
SUBRETINAL FIBROSIS ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
ULCER ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 4 FDA reports)
VERTEBROPLASTY ( 4 FDA reports)
VITREOUS DEGENERATION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONGENITAL ORAL MALFORMATION ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DISINHIBITION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
FORCEPS DELIVERY ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GOITRE ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 3 FDA reports)
HYPERPLASIA ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 3 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 3 FDA reports)
LESION EXCISION ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
NAIL DYSTROPHY ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEPSIS NEONATAL ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BONE OPERATION ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMA ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ECZEMA INFECTED ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
INFECTIOUS DISEASE CARRIER ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEITIS DEFORMANS ( 2 FDA reports)
OSTEORADIONECROSIS ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOPHERESIS ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
POOR DENTAL CONDITION ( 2 FDA reports)
POST-TRAUMATIC PAIN ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETROGNATHIA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPINAL ROD INSERTION ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AVERSION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLADDER NECROSIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONGENITAL SYPHILIS ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CSF LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILUTIONAL COAGULOPATHY ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPISPADIAS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETAL TOBACCO EXPOSURE ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NAEVUS FLAMMEUS ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLACENTA ACCRETA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTERIOR CAPSULOTOMY ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PUERPERAL PYREXIA ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE CHLORIDE INCREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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