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

DYSPNOEA ( 204 FDA reports)
ASTHMA ( 180 FDA reports)
NAUSEA ( 138 FDA reports)
DRUG INEFFECTIVE ( 115 FDA reports)
BACK PAIN ( 110 FDA reports)
DEPRESSION ( 106 FDA reports)
PAIN ( 103 FDA reports)
HEADACHE ( 98 FDA reports)
VOMITING ( 88 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 87 FDA reports)
FATIGUE ( 84 FDA reports)
DIZZINESS ( 79 FDA reports)
FALL ( 79 FDA reports)
LOSS OF CONSCIOUSNESS ( 78 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 77 FDA reports)
WEIGHT DECREASED ( 77 FDA reports)
ANXIETY ( 74 FDA reports)
DRUG DOSE OMISSION ( 74 FDA reports)
MALAISE ( 71 FDA reports)
CHEST DISCOMFORT ( 70 FDA reports)
ARTHRALGIA ( 69 FDA reports)
COUGH ( 67 FDA reports)
CHEST PAIN ( 66 FDA reports)
SYNCOPE ( 65 FDA reports)
OEDEMA PERIPHERAL ( 61 FDA reports)
PNEUMONIA ( 60 FDA reports)
BRONCHITIS ( 59 FDA reports)
DIARRHOEA ( 58 FDA reports)
INSOMNIA ( 58 FDA reports)
ANAEMIA ( 56 FDA reports)
ASTHENIA ( 54 FDA reports)
PYREXIA ( 54 FDA reports)
MYALGIA ( 51 FDA reports)
ABDOMINAL PAIN ( 50 FDA reports)
MYOCARDIAL INFARCTION ( 50 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 48 FDA reports)
PARAESTHESIA ( 47 FDA reports)
CONSTIPATION ( 45 FDA reports)
CONDITION AGGRAVATED ( 44 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 44 FDA reports)
HEART RATE IRREGULAR ( 43 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 42 FDA reports)
LABILE BLOOD PRESSURE ( 42 FDA reports)
HEART VALVE CALCIFICATION ( 40 FDA reports)
HEART VALVE INCOMPETENCE ( 40 FDA reports)
RADIOTHERAPY ( 40 FDA reports)
SINUSITIS ( 40 FDA reports)
SOMNOLENCE ( 40 FDA reports)
URINE ODOUR ABNORMAL ( 40 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 37 FDA reports)
OSTEOARTHRITIS ( 37 FDA reports)
RASH ( 37 FDA reports)
WHEEZING ( 37 FDA reports)
CEREBROVASCULAR ACCIDENT ( 36 FDA reports)
HYPERSENSITIVITY ( 36 FDA reports)
INJURY ( 36 FDA reports)
RENAL IMPAIRMENT ( 36 FDA reports)
SEPSIS ( 36 FDA reports)
FEELING ABNORMAL ( 35 FDA reports)
CONTUSION ( 34 FDA reports)
HYPERTENSION ( 34 FDA reports)
PAIN IN EXTREMITY ( 34 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 34 FDA reports)
DECREASED APPETITE ( 33 FDA reports)
BLOOD GLUCOSE INCREASED ( 32 FDA reports)
DIABETES MELLITUS ( 32 FDA reports)
IMPAIRED HEALING ( 32 FDA reports)
TREMOR ( 32 FDA reports)
ABDOMINAL PAIN UPPER ( 31 FDA reports)
MEMORY IMPAIRMENT ( 31 FDA reports)
NECK PAIN ( 31 FDA reports)
NERVOUSNESS ( 31 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 30 FDA reports)
PALPITATIONS ( 30 FDA reports)
ARTHRITIS ( 29 FDA reports)
URINARY TRACT INFECTION ( 29 FDA reports)
BLINDNESS ( 28 FDA reports)
CONFUSIONAL STATE ( 28 FDA reports)
URTICARIA ( 28 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 27 FDA reports)
FUNGAL INFECTION ( 27 FDA reports)
HYPOAESTHESIA ( 27 FDA reports)
MACULAR DEGENERATION ( 27 FDA reports)
RECTAL HAEMORRHAGE ( 27 FDA reports)
BLOOD PRESSURE INCREASED ( 26 FDA reports)
DYSPEPSIA ( 26 FDA reports)
MUSCULAR WEAKNESS ( 26 FDA reports)
OSTEONECROSIS ( 26 FDA reports)
RESPIRATORY FAILURE ( 26 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
DYSPHONIA ( 25 FDA reports)
HYPERGLYCAEMIA ( 25 FDA reports)
MUSCLE SPASMS ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
DYSPHAGIA ( 24 FDA reports)
HYPOTENSION ( 24 FDA reports)
SKIN ULCER ( 24 FDA reports)
ERYTHEMA ( 23 FDA reports)
NIGHT SWEATS ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
CHILLS ( 22 FDA reports)
CORONARY ARTERY DISEASE ( 22 FDA reports)
DYSGEUSIA ( 22 FDA reports)
HEPATIC STEATOSIS ( 22 FDA reports)
JOINT SWELLING ( 22 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 22 FDA reports)
ABDOMINAL DISCOMFORT ( 21 FDA reports)
HIATUS HERNIA ( 21 FDA reports)
HYPERLIPIDAEMIA ( 21 FDA reports)
PRURITUS ( 21 FDA reports)
SWELLING ( 21 FDA reports)
ABDOMINAL DISTENSION ( 20 FDA reports)
CELLULITIS ( 20 FDA reports)
DEATH ( 20 FDA reports)
DRUG HYPERSENSITIVITY ( 20 FDA reports)
ECONOMIC PROBLEM ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 20 FDA reports)
HAEMORRHAGE ( 20 FDA reports)
PRODUCT QUALITY ISSUE ( 20 FDA reports)
WEIGHT INCREASED ( 20 FDA reports)
BURSITIS ( 19 FDA reports)
NASAL CONGESTION ( 19 FDA reports)
OSTEOMYELITIS ( 19 FDA reports)
PAIN IN JAW ( 19 FDA reports)
PRODUCTIVE COUGH ( 19 FDA reports)
RESTLESS LEGS SYNDROME ( 19 FDA reports)
SUICIDAL IDEATION ( 19 FDA reports)
AMNESIA ( 18 FDA reports)
COLITIS ULCERATIVE ( 18 FDA reports)
DEAFNESS ( 18 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
DYSKINESIA ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
MIGRAINE ( 18 FDA reports)
URINARY INCONTINENCE ( 18 FDA reports)
WITHDRAWAL SYNDROME ( 18 FDA reports)
ABSCESS ( 17 FDA reports)
COLONIC POLYP ( 17 FDA reports)
DERMAL CYST ( 17 FDA reports)
FIBROMYALGIA ( 17 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
NEPHROLITHIASIS ( 17 FDA reports)
SINUS CONGESTION ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
ALOPECIA ( 16 FDA reports)
ANAPHYLACTIC REACTION ( 16 FDA reports)
ANGER ( 16 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
CHRONIC SINUSITIS ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 16 FDA reports)
GINGIVAL PAIN ( 16 FDA reports)
HAEMATOCHEZIA ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
JOINT SPRAIN ( 16 FDA reports)
LETHARGY ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 16 FDA reports)
PRIMARY SEQUESTRUM ( 16 FDA reports)
ROAD TRAFFIC ACCIDENT ( 16 FDA reports)
TACHYCARDIA ( 16 FDA reports)
TENDON RUPTURE ( 16 FDA reports)
ANOREXIA ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 15 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
BONE DISORDER ( 15 FDA reports)
BRONCHOSPASM ( 15 FDA reports)
CARDIAC DISORDER ( 15 FDA reports)
CYANOSIS ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 15 FDA reports)
DIVERTICULUM INTESTINAL ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
HAEMATOCRIT DECREASED ( 15 FDA reports)
LUNG DISORDER ( 15 FDA reports)
PERIODONTITIS ( 15 FDA reports)
PRURITUS GENERALISED ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
RHINORRHOEA ( 15 FDA reports)
RIB FRACTURE ( 15 FDA reports)
ROSACEA ( 15 FDA reports)
SEPTIC SHOCK ( 15 FDA reports)
TOOTHACHE ( 15 FDA reports)
TREATMENT NONCOMPLIANCE ( 15 FDA reports)
WHEELCHAIR USER ( 15 FDA reports)
ABDOMINAL TENDERNESS ( 14 FDA reports)
BLOOD UREA INCREASED ( 14 FDA reports)
CARDIO-RESPIRATORY ARREST ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
GASTRIC DISORDER ( 14 FDA reports)
GASTROENTERITIS ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
LIP ULCERATION ( 14 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
MUSCLE TWITCHING ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 14 FDA reports)
RESPIRATORY DISORDER ( 14 FDA reports)
ROTATOR CUFF SYNDROME ( 14 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 14 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 14 FDA reports)
ABASIA ( 13 FDA reports)
ANHEDONIA ( 13 FDA reports)
ATRIAL THROMBOSIS ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 13 FDA reports)
CEREBRAL INFARCTION ( 13 FDA reports)
DRY MOUTH ( 13 FDA reports)
FISTULA ( 13 FDA reports)
GASTROENTERITIS BACTERIAL ( 13 FDA reports)
GASTROINTESTINAL NECROSIS ( 13 FDA reports)
GINGIVITIS ( 13 FDA reports)
INFECTION ( 13 FDA reports)
INTENTIONAL DRUG MISUSE ( 13 FDA reports)
INTESTINAL PERFORATION ( 13 FDA reports)
IRRITABILITY ( 13 FDA reports)
MOOD SWINGS ( 13 FDA reports)
ORAL HERPES ( 13 FDA reports)
PARALYSIS ( 13 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
VISUAL IMPAIRMENT ( 13 FDA reports)
ACIDOSIS ( 12 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 12 FDA reports)
CATARACT ( 12 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
EXTREMITY NECROSIS ( 12 FDA reports)
EYELID OEDEMA ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
GASTROINTESTINAL DISORDER ( 12 FDA reports)
GINGIVAL ERYTHEMA ( 12 FDA reports)
GINGIVAL OEDEMA ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 12 FDA reports)
LYMPHADENOPATHY ( 12 FDA reports)
MASTOCYTOSIS ( 12 FDA reports)
MULTIPLE ALLERGIES ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
NEUROPATHY PERIPHERAL ( 12 FDA reports)
OESOPHAGITIS ( 12 FDA reports)
PANCREATITIS ( 12 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
POOR DENTAL CONDITION ( 12 FDA reports)
PROCTALGIA ( 12 FDA reports)
SKIN NECROSIS ( 12 FDA reports)
SLEEP APNOEA SYNDROME ( 12 FDA reports)
TENDONITIS ( 12 FDA reports)
URINARY RETENTION ( 12 FDA reports)
VERTIGO ( 12 FDA reports)
VISION BLURRED ( 12 FDA reports)
VISUAL ACUITY REDUCED ( 12 FDA reports)
ANGINA PECTORIS ( 11 FDA reports)
ARTHRITIS INFECTIVE ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 11 FDA reports)
CANDIDIASIS ( 11 FDA reports)
CHOKING ( 11 FDA reports)
COMA ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
INFUSION RELATED REACTION ( 11 FDA reports)
INTESTINAL RESECTION ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
OSTEONECROSIS OF JAW ( 11 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 11 FDA reports)
WOUND INFECTION ( 11 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 10 FDA reports)
ARTHROPATHY ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
BURNING SENSATION ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
CHOLECYSTITIS ACUTE ( 10 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
COLITIS ( 10 FDA reports)
DEMENTIA ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
EMOTIONAL DISORDER ( 10 FDA reports)
GOUT ( 10 FDA reports)
HAEMANGIOMA ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
INCORRECT DOSE ADMINISTERED ( 10 FDA reports)
LEG AMPUTATION ( 10 FDA reports)
LENTIGO ( 10 FDA reports)
LIMB INJURY ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
NOCTURIA ( 10 FDA reports)
OFF LABEL USE ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
RESPIRATORY TRACT CONGESTION ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
ANGIOMYOLIPOMA ( 9 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 9 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 9 FDA reports)
BONE DEBRIDEMENT ( 9 FDA reports)
BONE PAIN ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
DIVERTICULUM ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
FEAR ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
NEURALGIA ( 9 FDA reports)
ORAL INFECTION ( 9 FDA reports)
PRURITUS ANI ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
PYELONEPHRITIS ( 9 FDA reports)
RESTLESSNESS ( 9 FDA reports)
RHINITIS ALLERGIC ( 9 FDA reports)
SLEEP DISORDER ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 8 FDA reports)
BONE LESION ( 8 FDA reports)
CARDIAC MURMUR ( 8 FDA reports)
COSTOCHONDRITIS ( 8 FDA reports)
CRYING ( 8 FDA reports)
DECREASED INTEREST ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DIABETIC NEUROPATHY ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
EOSINOPHIL COUNT INCREASED ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
GINGIVAL ULCERATION ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
LACUNAR INFARCTION ( 8 FDA reports)
LIVER TRANSPLANT ( 8 FDA reports)
LUNG HYPERINFLATION ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PEPTIC ULCER ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
SINUS DISORDER ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
SNORING ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
SPINAL OSTEOARTHRITIS ( 8 FDA reports)
TENSION HEADACHE ( 8 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 8 FDA reports)
THERAPY NON-RESPONDER ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ANAL FISSURE ( 7 FDA reports)
APHASIA ( 7 FDA reports)
BACK INJURY ( 7 FDA reports)
DRUG INTOLERANCE ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
HEPATIC CYST ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYDROCELE ( 7 FDA reports)
HYPOPNOEA ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
JAUNDICE ( 7 FDA reports)
LACERATION ( 7 FDA reports)
MENINGITIS ASEPTIC ( 7 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
PENIS DISORDER ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PILONIDAL CYST ( 7 FDA reports)
PLEURITIC PAIN ( 7 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SKIN NODULE ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CYSTOCELE ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FLUID OVERLOAD ( 6 FDA reports)
FOOT FRACTURE ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GENERALISED OEDEMA ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
OBESITY ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
SENSORY LEVEL ABNORMAL ( 6 FDA reports)
SPINAL COMPRESSION FRACTURE ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
THYROID NEOPLASM ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
APNOEA ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 5 FDA reports)
CHOLECYSTECTOMY ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
COLON CANCER STAGE IV ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GOITRE ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
IMMUNOGLOBULINS DECREASED ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
RADICULITIS LUMBOSACRAL ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
STRESS ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
THIRST ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
VENOUS STASIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ANXIETY DISORDER ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
APHONIA ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
EXPOSED BONE IN JAW ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INGROWING NAIL ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SCROTAL CYST ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SEMINAL VESICULITIS ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SOMNAMBULISM ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SURGERY ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAL DISCOMFORT ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BUNION ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
CAROTID BRUIT ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLON GANGRENE ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CYST ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FEAR OF FALLING ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFECTED VARICOSE VEIN ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
JOINT LOCK ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MYCOTIC ALLERGY ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEURITIS ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PSEUDOPOLYPOSIS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TOOTH LOSS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
ULCER ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN LOBECTOMY ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE DEGENERATIVE DISORDER ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC URTICARIA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE WARMTH ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LID LAG ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODULE ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOPOLYP ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENSION ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOPEDIC EXAMINATION ABNORMAL ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC DEFORMITY ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEMINAL VESICULAR DISORDER ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SPERMATORRHOEA ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STUPOR ( 1 FDA reports)
STURGE-WEBER SYNDROME ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH ANKYLOSIS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOCELE REPAIR ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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