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

PAIN ( 246 FDA reports)
DYSPNOEA ( 235 FDA reports)
DIARRHOEA ( 233 FDA reports)
PYREXIA ( 224 FDA reports)
NAUSEA ( 186 FDA reports)
PRURITUS ( 186 FDA reports)
PNEUMONIA ( 177 FDA reports)
RENAL FAILURE ACUTE ( 167 FDA reports)
VOMITING ( 162 FDA reports)
ABDOMINAL PAIN ( 159 FDA reports)
ANXIETY ( 155 FDA reports)
DRUG INTERACTION ( 154 FDA reports)
RASH ( 153 FDA reports)
HYPOTENSION ( 126 FDA reports)
DIZZINESS ( 124 FDA reports)
COUGH ( 115 FDA reports)
HEADACHE ( 114 FDA reports)
ABDOMINAL PAIN UPPER ( 113 FDA reports)
ARTHRALGIA ( 113 FDA reports)
BACK PAIN ( 113 FDA reports)
CHEST PAIN ( 111 FDA reports)
URINARY TRACT INFECTION ( 107 FDA reports)
ATRIAL FIBRILLATION ( 101 FDA reports)
OEDEMA PERIPHERAL ( 100 FDA reports)
ASTHENIA ( 97 FDA reports)
FATIGUE ( 97 FDA reports)
CHOLELITHIASIS ( 95 FDA reports)
JAUNDICE ( 91 FDA reports)
DEPRESSION ( 90 FDA reports)
INJURY ( 89 FDA reports)
MALAISE ( 89 FDA reports)
ANAEMIA ( 88 FDA reports)
PULMONARY EMBOLISM ( 88 FDA reports)
STEVENS-JOHNSON SYNDROME ( 84 FDA reports)
PAIN IN EXTREMITY ( 83 FDA reports)
ERYTHEMA ( 81 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 81 FDA reports)
DYSPHAGIA ( 80 FDA reports)
OSTEONECROSIS OF JAW ( 80 FDA reports)
DRUG INEFFECTIVE ( 78 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 75 FDA reports)
BLOOD CREATININE INCREASED ( 72 FDA reports)
DEHYDRATION ( 71 FDA reports)
ANAPHYLACTIC REACTION ( 69 FDA reports)
SEPSIS ( 69 FDA reports)
CONFUSIONAL STATE ( 68 FDA reports)
URTICARIA ( 67 FDA reports)
DEATH ( 66 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 65 FDA reports)
HYPERSENSITIVITY ( 65 FDA reports)
LYMPHADENOPATHY ( 65 FDA reports)
RENAL FAILURE ( 65 FDA reports)
HAEMOGLOBIN DECREASED ( 63 FDA reports)
FALL ( 62 FDA reports)
NEUTROPENIA ( 62 FDA reports)
SINUSITIS ( 62 FDA reports)
SYNCOPE ( 62 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 61 FDA reports)
THROMBOCYTOPENIA ( 60 FDA reports)
WEIGHT DECREASED ( 60 FDA reports)
DECREASED APPETITE ( 58 FDA reports)
MUSCULOSKELETAL PAIN ( 58 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 57 FDA reports)
BRONCHITIS ( 57 FDA reports)
HEPATITIS CHOLESTATIC ( 57 FDA reports)
HYPERHIDROSIS ( 56 FDA reports)
OSTEOARTHRITIS ( 56 FDA reports)
PANCYTOPENIA ( 55 FDA reports)
VISION BLURRED ( 55 FDA reports)
ECZEMA ( 54 FDA reports)
OSTEOMYELITIS ( 54 FDA reports)
SINUS DISORDER ( 54 FDA reports)
CARDIAC ARREST ( 53 FDA reports)
CHOLECYSTITIS CHRONIC ( 53 FDA reports)
CONDITION AGGRAVATED ( 53 FDA reports)
HYPERTENSION ( 53 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 53 FDA reports)
PARAESTHESIA ( 53 FDA reports)
CEREBROVASCULAR ACCIDENT ( 52 FDA reports)
EMOTIONAL DISTRESS ( 52 FDA reports)
HYPOAESTHESIA ( 52 FDA reports)
LOSS OF CONSCIOUSNESS ( 52 FDA reports)
MENTAL DISORDER ( 52 FDA reports)
DEEP VEIN THROMBOSIS ( 51 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 51 FDA reports)
PLEURAL EFFUSION ( 50 FDA reports)
CATARACT ( 49 FDA reports)
RASH MACULO-PAPULAR ( 48 FDA reports)
CHOLESTASIS ( 47 FDA reports)
OSTEOPENIA ( 47 FDA reports)
BLOOD BILIRUBIN INCREASED ( 46 FDA reports)
CONSTIPATION ( 46 FDA reports)
LUNG INFILTRATION ( 46 FDA reports)
TACHYCARDIA ( 46 FDA reports)
BONE DISORDER ( 45 FDA reports)
CHROMATURIA ( 45 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 45 FDA reports)
RASH PRURITIC ( 44 FDA reports)
RESPIRATORY FAILURE ( 44 FDA reports)
DIVERTICULUM ( 43 FDA reports)
SPINAL OSTEOARTHRITIS ( 43 FDA reports)
ILEUS ( 42 FDA reports)
MUSCLE SPASMS ( 42 FDA reports)
ROTATOR CUFF SYNDROME ( 42 FDA reports)
ORAL PAIN ( 41 FDA reports)
ARTHRITIS ( 40 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 40 FDA reports)
LIVER INJURY ( 40 FDA reports)
NECK PAIN ( 40 FDA reports)
OVERDOSE ( 40 FDA reports)
ANGIOEDEMA ( 39 FDA reports)
CONVULSION ( 39 FDA reports)
MUCOSAL INFLAMMATION ( 39 FDA reports)
SWELLING FACE ( 39 FDA reports)
INFLAMMATION ( 38 FDA reports)
INSOMNIA ( 38 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 38 FDA reports)
METASTASES TO BONE ( 38 FDA reports)
PULMONARY OEDEMA ( 38 FDA reports)
MUSCULAR WEAKNESS ( 37 FDA reports)
MYALGIA ( 37 FDA reports)
MYOCARDIAL INFARCTION ( 37 FDA reports)
NEUROPATHY PERIPHERAL ( 37 FDA reports)
SWELLING ( 37 FDA reports)
ATELECTASIS ( 36 FDA reports)
FEBRILE NEUTROPENIA ( 36 FDA reports)
HAEMOPTYSIS ( 36 FDA reports)
LEUKOPENIA ( 36 FDA reports)
SENSITIVITY OF TEETH ( 36 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 36 FDA reports)
CARDIAC FAILURE ( 35 FDA reports)
DRUG HYPERSENSITIVITY ( 35 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 35 FDA reports)
WHEEZING ( 35 FDA reports)
BONE PAIN ( 34 FDA reports)
DIPLOPIA ( 34 FDA reports)
HEPATITIS ( 34 FDA reports)
KYPHOSIS ( 34 FDA reports)
RASH GENERALISED ( 34 FDA reports)
BURSITIS ( 33 FDA reports)
GALLBLADDER DISORDER ( 33 FDA reports)
GASTROENTERITIS ( 33 FDA reports)
IMPAIRED HEALING ( 33 FDA reports)
RHABDOMYOLYSIS ( 33 FDA reports)
SKIN EXFOLIATION ( 33 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 33 FDA reports)
CELLULITIS ( 32 FDA reports)
DYSPEPSIA ( 32 FDA reports)
HEPATIC FAILURE ( 32 FDA reports)
HYDRONEPHROSIS ( 32 FDA reports)
HYPONATRAEMIA ( 32 FDA reports)
MULTI-ORGAN FAILURE ( 32 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 31 FDA reports)
CHEST DISCOMFORT ( 31 FDA reports)
CHILLS ( 31 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 31 FDA reports)
DYSGEUSIA ( 31 FDA reports)
DYSURIA ( 31 FDA reports)
ARTHROPATHY ( 30 FDA reports)
BLISTER ( 30 FDA reports)
CARDIOMEGALY ( 30 FDA reports)
CEREBRAL ATROPHY ( 30 FDA reports)
FISTULA ( 30 FDA reports)
HYPERCHOLESTEROLAEMIA ( 30 FDA reports)
UNRESPONSIVE TO STIMULI ( 30 FDA reports)
URINARY RETENTION ( 30 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 29 FDA reports)
DERMATITIS CONTACT ( 29 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 29 FDA reports)
FLUID OVERLOAD ( 29 FDA reports)
HAEMATURIA ( 29 FDA reports)
INFECTION ( 29 FDA reports)
LEFT ATRIAL DILATATION ( 29 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 29 FDA reports)
MULTIPLE MYELOMA ( 29 FDA reports)
NEOPLASM MALIGNANT ( 29 FDA reports)
ORAL DISORDER ( 29 FDA reports)
OROPHARYNGEAL PAIN ( 29 FDA reports)
SOMNOLENCE ( 29 FDA reports)
ABSCESS ( 28 FDA reports)
ANAPHYLACTIC SHOCK ( 28 FDA reports)
ANHEDONIA ( 28 FDA reports)
DRY MOUTH ( 28 FDA reports)
ENCEPHALOPATHY ( 28 FDA reports)
ERYTHEMA MULTIFORME ( 28 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 28 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 28 FDA reports)
OBESITY ( 28 FDA reports)
PETECHIAE ( 28 FDA reports)
VENTRICULAR TACHYCARDIA ( 28 FDA reports)
VITREOUS FLOATERS ( 28 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 27 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
HEPATOTOXICITY ( 27 FDA reports)
PAIN IN JAW ( 27 FDA reports)
PRIMARY SEQUESTRUM ( 27 FDA reports)
RADICULOPATHY ( 27 FDA reports)
RASH ERYTHEMATOUS ( 27 FDA reports)
ABDOMINAL PAIN LOWER ( 26 FDA reports)
APHASIA ( 26 FDA reports)
GAIT DISTURBANCE ( 26 FDA reports)
LUNG NEOPLASM ( 26 FDA reports)
OEDEMA ( 26 FDA reports)
RENAL FAILURE CHRONIC ( 26 FDA reports)
SPUTUM DISCOLOURED ( 26 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 25 FDA reports)
FAECES DISCOLOURED ( 25 FDA reports)
PALPITATIONS ( 25 FDA reports)
ABDOMINAL DISCOMFORT ( 24 FDA reports)
ACUTE HEPATIC FAILURE ( 24 FDA reports)
CYSTITIS ( 24 FDA reports)
GASTRITIS ( 24 FDA reports)
HALLUCINATION ( 24 FDA reports)
HEPATIC ENZYME INCREASED ( 24 FDA reports)
JAUNDICE CHOLESTATIC ( 24 FDA reports)
LIVER DISORDER ( 24 FDA reports)
MEDICATION ERROR ( 24 FDA reports)
PRESYNCOPE ( 24 FDA reports)
RESPIRATORY DISTRESS ( 24 FDA reports)
SKIN ULCER ( 24 FDA reports)
SUICIDAL IDEATION ( 24 FDA reports)
TOOTH FRACTURE ( 24 FDA reports)
TREMOR ( 24 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 23 FDA reports)
AGRANULOCYTOSIS ( 23 FDA reports)
CLOSTRIDIAL INFECTION ( 23 FDA reports)
DENTAL CARIES ( 23 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 23 FDA reports)
FEAR ( 23 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
HYPOKALAEMIA ( 23 FDA reports)
RENAL DISORDER ( 23 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 23 FDA reports)
UPPER LIMB FRACTURE ( 23 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
ABASIA ( 22 FDA reports)
BASAL CELL CARCINOMA ( 22 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 22 FDA reports)
CARDIO-RESPIRATORY ARREST ( 22 FDA reports)
DRY SKIN ( 22 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 22 FDA reports)
GLAUCOMA ( 22 FDA reports)
HEPATIC CYST ( 22 FDA reports)
KOUNIS SYNDROME ( 22 FDA reports)
MELAENA ( 22 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 22 FDA reports)
OTITIS MEDIA ( 22 FDA reports)
PURULENCE ( 22 FDA reports)
PURULENT DISCHARGE ( 22 FDA reports)
STAPHYLOCOCCAL INFECTION ( 22 FDA reports)
TOOTH INFECTION ( 22 FDA reports)
TOXIC SKIN ERUPTION ( 22 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 21 FDA reports)
CARDIAC DISORDER ( 21 FDA reports)
CHONDROMALACIA ( 21 FDA reports)
CYTOLYTIC HEPATITIS ( 21 FDA reports)
DILATATION VENTRICULAR ( 21 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 21 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 21 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
HEART RATE INCREASED ( 21 FDA reports)
HEPATOMEGALY ( 21 FDA reports)
HYPOXIA ( 21 FDA reports)
INFLUENZA ( 21 FDA reports)
LETHARGY ( 21 FDA reports)
METABOLIC ACIDOSIS ( 21 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 21 FDA reports)
ORTHOSTATIC HYPOTENSION ( 21 FDA reports)
PRODUCT QUALITY ISSUE ( 21 FDA reports)
RENAL CYST ( 21 FDA reports)
SUBCUTANEOUS NODULE ( 21 FDA reports)
WEIGHT INCREASED ( 21 FDA reports)
ABDOMINAL DISTENSION ( 20 FDA reports)
AGITATION ( 20 FDA reports)
APNOEA ( 20 FDA reports)
CHOLECYSTITIS ACUTE ( 20 FDA reports)
DECREASED INTEREST ( 20 FDA reports)
DERMATITIS ( 20 FDA reports)
EAR PAIN ( 20 FDA reports)
EOSINOPHILIA ( 20 FDA reports)
EXOSTOSIS ( 20 FDA reports)
HAEMORRHAGE ( 20 FDA reports)
HODGKIN'S DISEASE ( 20 FDA reports)
MASTICATION DISORDER ( 20 FDA reports)
MYASTHENIA GRAVIS ( 20 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 20 FDA reports)
NEUTROPENIC SEPSIS ( 20 FDA reports)
PLATELET COUNT DECREASED ( 20 FDA reports)
RENAL IMPAIRMENT ( 20 FDA reports)
RIB FRACTURE ( 20 FDA reports)
SEPTIC SHOCK ( 20 FDA reports)
SPINAL COMPRESSION FRACTURE ( 20 FDA reports)
VERTIGO ( 20 FDA reports)
APPENDICECTOMY ( 19 FDA reports)
ASTHMA ( 19 FDA reports)
BIOPSY BONE MARROW ( 19 FDA reports)
BRONCHIAL SECRETION RETENTION ( 19 FDA reports)
CERVICAL CORD COMPRESSION ( 19 FDA reports)
CHRONIC SINUSITIS ( 19 FDA reports)
CONJUNCTIVITIS ( 19 FDA reports)
DENTAL PULP DISORDER ( 19 FDA reports)
DEVICE MALFUNCTION ( 19 FDA reports)
DYSPHONIA ( 19 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 19 FDA reports)
HIATUS HERNIA ( 19 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 19 FDA reports)
LUDWIG ANGINA ( 19 FDA reports)
METASTASES TO LIVER ( 19 FDA reports)
MITRAL VALVE INCOMPETENCE ( 19 FDA reports)
NASAL CONGESTION ( 19 FDA reports)
OXYGEN SATURATION DECREASED ( 19 FDA reports)
PULMONARY HYPERTENSION ( 19 FDA reports)
SPINAL FUSION ACQUIRED ( 19 FDA reports)
TENDERNESS ( 19 FDA reports)
TOOTH DISORDER ( 19 FDA reports)
TRANSAMINASES INCREASED ( 19 FDA reports)
VISUAL IMPAIRMENT ( 19 FDA reports)
ABDOMINAL HERNIA ( 18 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 18 FDA reports)
BRADYCARDIA ( 18 FDA reports)
BRONCHOSPASM ( 18 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 18 FDA reports)
DERMATITIS EXFOLIATIVE ( 18 FDA reports)
ERYSIPELAS ( 18 FDA reports)
EXFOLIATIVE RASH ( 18 FDA reports)
FUNGAL INFECTION ( 18 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 18 FDA reports)
HEPATITIS ACUTE ( 18 FDA reports)
LUNG INFECTION ( 18 FDA reports)
LYMPHOEDEMA ( 18 FDA reports)
MENISCUS LESION ( 18 FDA reports)
MIGRAINE ( 18 FDA reports)
NASOPHARYNGITIS ( 18 FDA reports)
NECROSIS ( 18 FDA reports)
PANCREATITIS ( 18 FDA reports)
PSYCHOTIC DISORDER ( 18 FDA reports)
PULMONARY CONGESTION ( 18 FDA reports)
PULMONARY FIBROSIS ( 18 FDA reports)
PURPURA ( 18 FDA reports)
RESPIRATORY TRACT INFECTION ( 18 FDA reports)
RETINAL HAEMORRHAGE ( 18 FDA reports)
SCAB ( 18 FDA reports)
SINUS TACHYCARDIA ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
VENOUS THROMBOSIS ( 18 FDA reports)
VITREOUS DETACHMENT ( 18 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
CAROTID ARTERY STENOSIS ( 17 FDA reports)
FACE OEDEMA ( 17 FDA reports)
FLANK PAIN ( 17 FDA reports)
GINGIVAL BLEEDING ( 17 FDA reports)
GINGIVAL ULCERATION ( 17 FDA reports)
HAEMATEMESIS ( 17 FDA reports)
HYPERLIPIDAEMIA ( 17 FDA reports)
HYPOGLYCAEMIA ( 17 FDA reports)
MENINGITIS ASEPTIC ( 17 FDA reports)
MOOD SWINGS ( 17 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 17 FDA reports)
SINUS POLYP DEGENERATION ( 17 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
INFLUENZA LIKE ILLNESS ( 16 FDA reports)
JOINT DISLOCATION ( 16 FDA reports)
JOINT SWELLING ( 16 FDA reports)
MALIGNANT MELANOMA IN SITU ( 16 FDA reports)
MYOPATHY ( 16 FDA reports)
OSTEOPOROSIS ( 16 FDA reports)
PHARYNGEAL OEDEMA ( 16 FDA reports)
PROTEINURIA ( 16 FDA reports)
SKIN LESION ( 16 FDA reports)
SLEEP DISORDER ( 16 FDA reports)
VASCULITIS ( 16 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 16 FDA reports)
CLAVICLE FRACTURE ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
DISORIENTATION ( 15 FDA reports)
DRY EYE ( 15 FDA reports)
EAR INFECTION ( 15 FDA reports)
EJECTION FRACTION DECREASED ( 15 FDA reports)
HAEMORRHOIDS ( 15 FDA reports)
HEMIPARESIS ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
LUMBAR SPINAL STENOSIS ( 15 FDA reports)
MASTITIS ( 15 FDA reports)
MEMORY IMPAIRMENT ( 15 FDA reports)
ODYNOPHAGIA ( 15 FDA reports)
OLIGURIA ( 15 FDA reports)
PARANOIA ( 15 FDA reports)
RHINORRHOEA ( 15 FDA reports)
ROAD TRAFFIC ACCIDENT ( 15 FDA reports)
SCAR ( 15 FDA reports)
SCOLIOSIS ( 15 FDA reports)
THROMBOSIS ( 15 FDA reports)
WOUND INFECTION ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
ANGER ( 14 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 14 FDA reports)
BRONCHIOLITIS ( 14 FDA reports)
CARDIOMYOPATHY ( 14 FDA reports)
COLITIS ( 14 FDA reports)
DEBRIDEMENT ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DISEASE PROGRESSION ( 14 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
HAEMATOMA ( 14 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
MENTAL STATUS CHANGES ( 14 FDA reports)
NEUROENDOCRINE CARCINOMA ( 14 FDA reports)
OSTEITIS ( 14 FDA reports)
PHARYNGITIS ( 14 FDA reports)
PRODUCTIVE COUGH ( 14 FDA reports)
PYODERMA GANGRENOSUM ( 14 FDA reports)
SHOCK ( 14 FDA reports)
SUDDEN DEATH ( 14 FDA reports)
SYNOVIAL CYST ( 14 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 14 FDA reports)
AMNESIA ( 13 FDA reports)
ANKLE FRACTURE ( 13 FDA reports)
APPENDICITIS PERFORATED ( 13 FDA reports)
ARRHYTHMIA ( 13 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 13 FDA reports)
BIPOLAR DISORDER ( 13 FDA reports)
BONE SCAN ABNORMAL ( 13 FDA reports)
COLONIC POLYP ( 13 FDA reports)
COMA ( 13 FDA reports)
CONJUNCTIVOCHALASIS ( 13 FDA reports)
CONNECTIVE TISSUE DISORDER ( 13 FDA reports)
CORNEAL DYSTROPHY ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
DISABILITY ( 13 FDA reports)
DRUG TOXICITY ( 13 FDA reports)
FACIAL PAIN ( 13 FDA reports)
FOOT FRACTURE ( 13 FDA reports)
GLARE ( 13 FDA reports)
HERPES ZOSTER ( 13 FDA reports)
INTERTRIGO ( 13 FDA reports)
IRRITABILITY ( 13 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 13 FDA reports)
LYMPHOMA ( 13 FDA reports)
MELANOSIS COLI ( 13 FDA reports)
MICROANGIOPATHY ( 13 FDA reports)
NEOPLASM PROGRESSION ( 13 FDA reports)
NIGHT SWEATS ( 13 FDA reports)
OSTEOSCLEROSIS ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
POOR QUALITY SLEEP ( 13 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
RASH PUSTULAR ( 13 FDA reports)
RESORPTION BONE INCREASED ( 13 FDA reports)
SPINAL DISORDER ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
TINNITUS ( 13 FDA reports)
TONSILLITIS ( 13 FDA reports)
ULNAR NEURITIS ( 13 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 13 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 13 FDA reports)
ABDOMINAL ABSCESS ( 12 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
AGGRESSION ( 12 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
BILIARY COLIC ( 12 FDA reports)
BREAST CANCER RECURRENT ( 12 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 12 FDA reports)
CHOLECYSTITIS ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CYANOSIS ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
ECONOMIC PROBLEM ( 12 FDA reports)
EYE SWELLING ( 12 FDA reports)
FEELING HOT ( 12 FDA reports)
FOETAL DISTRESS SYNDROME ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HYPERBILIRUBINAEMIA ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
IMMOBILE ( 12 FDA reports)
LUNG CONSOLIDATION ( 12 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 12 FDA reports)
METASTATIC NEOPLASM ( 12 FDA reports)
MONOCYTE COUNT INCREASED ( 12 FDA reports)
MOUTH ULCERATION ( 12 FDA reports)
ORAL CANDIDIASIS ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
PNEUMOTHORAX ( 12 FDA reports)
POLLAKIURIA ( 12 FDA reports)
PROSTATOMEGALY ( 12 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 12 FDA reports)
PYELONEPHRITIS ( 12 FDA reports)
RADIATION OESOPHAGITIS ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
REFLUX OESOPHAGITIS ( 12 FDA reports)
RHINITIS ALLERGIC ( 12 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 12 FDA reports)
ACUTE SINUSITIS ( 11 FDA reports)
ADVERSE DRUG REACTION ( 11 FDA reports)
ANURIA ( 11 FDA reports)
ARTERIOSCLEROSIS ( 11 FDA reports)
BARRETT'S OESOPHAGUS ( 11 FDA reports)
BODY TEMPERATURE INCREASED ( 11 FDA reports)
BRONCHITIS CHRONIC ( 11 FDA reports)
CONTUSION ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
DRUG DISPENSING ERROR ( 11 FDA reports)
DYSPNOEA EXERTIONAL ( 11 FDA reports)
FLATULENCE ( 11 FDA reports)
FLUSHING ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HEPATIC ENCEPHALOPATHY ( 11 FDA reports)
HYPERGLYCAEMIA ( 11 FDA reports)
HYPERREFLEXIA ( 11 FDA reports)
HYPERTHYROIDISM ( 11 FDA reports)
ILEITIS ( 11 FDA reports)
INCISION SITE INFECTION ( 11 FDA reports)
LACTIC ACIDOSIS ( 11 FDA reports)
LOBAR PNEUMONIA ( 11 FDA reports)
METASTASES TO SPINE ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
RASH MACULAR ( 11 FDA reports)
SWOLLEN TONGUE ( 11 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 11 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ADVERSE EVENT ( 10 FDA reports)
ANAL FISSURE ( 10 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
BLOOD URINE PRESENT ( 10 FDA reports)
BONE LOSS ( 10 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
DEFORMITY ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
EATING DISORDER ( 10 FDA reports)
ECCHYMOSIS ( 10 FDA reports)
ECZEMA EYELIDS ( 10 FDA reports)
ENTEROCOCCAL INFECTION ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
FEELING COLD ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HERPES SIMPLEX ( 10 FDA reports)
HUMERUS FRACTURE ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 10 FDA reports)
KIDNEY INFECTION ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LIP SWELLING ( 10 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
MEDIASTINUM NEOPLASM ( 10 FDA reports)
METASTASES TO LUNG ( 10 FDA reports)
NECK MASS ( 10 FDA reports)
NEGATIVE THOUGHTS ( 10 FDA reports)
OESOPHAGEAL PAIN ( 10 FDA reports)
PHLEBITIS ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
QUALITY OF LIFE DECREASED ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
TENDON DISORDER ( 10 FDA reports)
THYROID NEOPLASM ( 10 FDA reports)
URINE ANALYSIS ABNORMAL ( 10 FDA reports)
VIRAL PHARYNGITIS ( 10 FDA reports)
ALOPECIA ( 9 FDA reports)
ANGIONEUROTIC OEDEMA ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 9 FDA reports)
ARTHROPOD BITE ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BILIARY DYSKINESIA ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
CACHEXIA ( 9 FDA reports)
CANDIDIASIS ( 9 FDA reports)
CIRCULATORY COLLAPSE ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
COMPRESSION FRACTURE ( 9 FDA reports)
CRYING ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DRUG RESISTANCE ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
DYSLIPIDAEMIA ( 9 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 9 FDA reports)
ESCHERICHIA INFECTION ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
HEPATOCELLULAR INJURY ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
IMPULSE-CONTROL DISORDER ( 9 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 9 FDA reports)
ISCHAEMIC STROKE ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
MUSCLE TIGHTNESS ( 9 FDA reports)
MYOCLONUS ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
NOCTURIA ( 9 FDA reports)
OESOPHAGITIS ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 9 FDA reports)
PLATELET COUNT INCREASED ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
RESTLESSNESS ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 9 FDA reports)
STRESS ( 9 FDA reports)
TENDON RUPTURE ( 9 FDA reports)
UNEVALUABLE EVENT ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
ACIDOSIS ( 8 FDA reports)
AZOTAEMIA ( 8 FDA reports)
BIOPSY LYMPH GLAND ( 8 FDA reports)
BONE MARROW FAILURE ( 8 FDA reports)
BONE MARROW TOXICITY ( 8 FDA reports)
BONE TRIMMING ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 8 FDA reports)
CERVICAL SPINAL STENOSIS ( 8 FDA reports)
COLD SWEAT ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 8 FDA reports)
EMOTIONAL DISORDER ( 8 FDA reports)
ENDOCARDITIS ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 8 FDA reports)
EYELID OPERATION ( 8 FDA reports)
FAECES PALE ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
GENERALISED ERYTHEMA ( 8 FDA reports)
GOUT ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 8 FDA reports)
HYPOVOLAEMIC SHOCK ( 8 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LYMPHOPENIA ( 8 FDA reports)
MASS EXCISION ( 8 FDA reports)
MAXILLOFACIAL OPERATION ( 8 FDA reports)
METASTASES TO EYE ( 8 FDA reports)
METASTASES TO MENINGES ( 8 FDA reports)
MUCOSAL EROSION ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
OLIGOHYDRAMNIOS ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
ORAL NEOPLASM ( 8 FDA reports)
PALLOR ( 8 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
PROTEIN URINE PRESENT ( 8 FDA reports)
RASH MORBILLIFORM ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
RENAL MASS ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
SINUS ANTROSTOMY ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
SINUS OPERATION ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
SPONDYLOLISTHESIS ( 8 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 8 FDA reports)
STARING ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
STRABISMUS ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 8 FDA reports)
URINARY FISTULA ( 8 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 8 FDA reports)
ABSCESS NECK ( 7 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 7 FDA reports)
ANAL ATRESIA ( 7 FDA reports)
ANGINA UNSTABLE ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 7 FDA reports)
BEDRIDDEN ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CERVICAL DYSPLASIA ( 7 FDA reports)
CHOLANGITIS ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
ELECTROLYTE IMBALANCE ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
ERYTHEMA NODOSUM ( 7 FDA reports)
FACET JOINT SYNDROME ( 7 FDA reports)
GINGIVAL DISORDER ( 7 FDA reports)
GOITRE ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HEPATIC MASS ( 7 FDA reports)
HEPATIC NECROSIS ( 7 FDA reports)
HYPERTHERMIA MALIGNANT ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
LACERATION ( 7 FDA reports)
LORDOSIS ( 7 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
METAPLASIA ( 7 FDA reports)
METASTASES TO LYMPH NODES ( 7 FDA reports)
METASTASIS ( 7 FDA reports)
NEPHROPATHY ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
OPHTHALMOPLEGIA ( 7 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 7 FDA reports)
PANCREATITIS ACUTE ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
RELAPSING FEVER ( 7 FDA reports)
SKIN BURNING SENSATION ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
STUPOR ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
TENOSYNOVITIS STENOSANS ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
TOXOPLASMOSIS ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
VESTIBULAR DISORDER ( 7 FDA reports)
VULVITIS ( 7 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 7 FDA reports)
YELLOW SKIN ( 7 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ABSCESS DRAINAGE ( 6 FDA reports)
ACCIDENT AT WORK ( 6 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
ANORECTAL DISORDER ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CHOLESTATIC LIVER INJURY ( 6 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 6 FDA reports)
DEAFNESS NEUROSENSORY ( 6 FDA reports)
DEATH NEONATAL ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DERMATITIS ALLERGIC ( 6 FDA reports)
DIABETIC COMPLICATION ( 6 FDA reports)
DIALYSIS ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DISINHIBITION ( 6 FDA reports)
ENDODONTIC PROCEDURE ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
EXPOSED BONE IN JAW ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GRAFT DYSFUNCTION ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INGROWING NAIL ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
KLEBSIELLA INFECTION ( 6 FDA reports)
KNEE OPERATION ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
POOR VENOUS ACCESS ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
POSTNASAL DRIP ( 6 FDA reports)
PREMATURE DELIVERY ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 6 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
RHINITIS ( 6 FDA reports)
SEROTONIN SYNDROME ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
SKIN TEST POSITIVE ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SPEECH REHABILITATION ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
STATUS EPILEPTICUS ( 6 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 6 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TONGUE DISORDER ( 6 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 6 FDA reports)
TREATMENT FAILURE ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
URETERIC STENOSIS ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACTINIC KERATOSIS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ANGIOPATHY ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
AORTIC STENOSIS ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
APPETITE DISORDER ( 5 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BREAST ABSCESS ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CONGENITAL ACROCHORDON ( 5 FDA reports)
CONGENITAL HEARING DISORDER ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FACIAL DYSMORPHISM ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
H1N1 INFLUENZA ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
HYPOSPADIAS ( 5 FDA reports)
IMPETIGO ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
INTESTINAL ISCHAEMIA ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
JAUNDICE NEONATAL ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LOCALISED INFECTION ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MIXED LIVER INJURY ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MUSCLE NECROSIS ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OCULAR SURFACE DISEASE ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
POLYNEUROPATHY ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PULMONARY GRANULOMA ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
RIB HYPOPLASIA ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SINUS CONGESTION ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SURGERY ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
URETERAL NECROSIS ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
URINOMA ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLADDER TAMPONADE ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CERUMEN IMPACTION ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
DIABETIC FOOT ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 4 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EMPYEMA ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HERPES OPHTHALMIC ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NEUROFIBROMA ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OSTEOLYSIS ( 4 FDA reports)
PENILE OEDEMA ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PERSISTENT LEFT SUPERIOR VENA CAVA ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLAGIOCEPHALY ( 4 FDA reports)
POISONING ( 4 FDA reports)
POSTRENAL FAILURE ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
RALES ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RENAL SURGERY ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN INFECTION ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SNORING ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TOE DEFORMITY ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TORTICOLLIS ( 4 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TYPE I HYPERSENSITIVITY ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VASOCONSTRICTION ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ACUTE TONSILLITIS ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAEMIA NEONATAL ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
APATHY ( 3 FDA reports)
APHONIA ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
CERVICAL MYELOPATHY ( 3 FDA reports)
CHOLANGITIS SCLEROSING ( 3 FDA reports)
CHOLESTEROSIS ( 3 FDA reports)
CHOLURIA ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CROUP INFECTIOUS ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMANGIOMA ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HYDROPS FOETALIS ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LIVE BIRTH ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PRODUCT COLOUR ISSUE ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL FAILURE NEONATAL ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SALIVARY GLAND MASS ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SOPOR ( 3 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACNE ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRYOGLOBULINS PRESENT ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 2 FDA reports)
ENDOMETRIAL ATROPHY ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
GROSS MOTOR DELAY ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT DISLOCATION REDUCTION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MACULE ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NEUROMUSCULAR BLOCKADE ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
OROPHARYNGITIS FUNGAL ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OVARIAN ATROPHY ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RHODOCOCCUS INFECTION ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
SUBACUTE HEPATIC FAILURE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TERTIARY SYPHILIS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THYROID ATROPHY ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
ULCER ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
UROGENITAL DISORDER ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMNIOTIC FLUID INDEX ABNORMAL ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANGIOSARCOMA RECURRENT ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR CANAL ( 1 FDA reports)
ATROPHIC GLOSSITIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BILE CULTURE POSITIVE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAPILLARITIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMYOPATHY NEONATAL ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLANGITIS CHRONIC ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
COAGULATION DISORDER NEONATAL ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPLEMENT FACTOR C1 DECREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL URETERIC ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEFICIENCY OF BILE SECRETION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DUCTUS ARTERIOSUS STENOSIS FOETAL ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DUST INHALATION PNEUMOPATHY ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR CANAL STENOSIS ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EUSTACHIAN TUBE STENOSIS ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALACTOSTASIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C RNA FLUCTUATION ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFANTILE SPITTING UP ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAUTERINE INFECTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOSIS OBTURANS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NAIL BED INFECTION FUNGAL ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC RASH ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
URETHRAL DILATATION ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINAL SWELLING ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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