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

DIZZINESS ( 73 FDA reports)
DYSPNOEA ( 68 FDA reports)
DEPRESSION ( 65 FDA reports)
FATIGUE ( 64 FDA reports)
PAIN ( 62 FDA reports)
ASTHMA ( 58 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 58 FDA reports)
ANXIETY ( 57 FDA reports)
CONSTIPATION ( 57 FDA reports)
HYPOAESTHESIA ( 57 FDA reports)
CHEST PAIN ( 56 FDA reports)
ABDOMINAL PAIN ( 51 FDA reports)
FALL ( 50 FDA reports)
NAUSEA ( 49 FDA reports)
ARTHRALGIA ( 48 FDA reports)
COUGH ( 48 FDA reports)
ASTHENIA ( 47 FDA reports)
MUSCLE SPASMS ( 47 FDA reports)
SYNCOPE ( 46 FDA reports)
ANAEMIA ( 44 FDA reports)
DIARRHOEA ( 43 FDA reports)
PARAESTHESIA ( 43 FDA reports)
WEIGHT DECREASED ( 41 FDA reports)
OSTEOPOROSIS ( 39 FDA reports)
PYREXIA ( 38 FDA reports)
HAEMORRHOIDS ( 36 FDA reports)
HEADACHE ( 35 FDA reports)
PAIN IN EXTREMITY ( 35 FDA reports)
HAEMOGLOBIN DECREASED ( 34 FDA reports)
HYPOTENSION ( 34 FDA reports)
DRUG INEFFECTIVE ( 33 FDA reports)
URINARY TRACT INFECTION ( 33 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 32 FDA reports)
LOSS OF CONSCIOUSNESS ( 32 FDA reports)
MYALGIA ( 32 FDA reports)
GAIT DISTURBANCE ( 31 FDA reports)
TINNITUS ( 31 FDA reports)
BASAL CELL CARCINOMA ( 30 FDA reports)
BURNING SENSATION ( 30 FDA reports)
CONDITION AGGRAVATED ( 30 FDA reports)
HALLUCINATION ( 30 FDA reports)
RENAL IMPAIRMENT ( 30 FDA reports)
CONVULSION ( 29 FDA reports)
DRY SKIN ( 29 FDA reports)
INSOMNIA ( 29 FDA reports)
VISUAL ACUITY REDUCED ( 29 FDA reports)
DYSURIA ( 28 FDA reports)
EXOSTOSIS ( 28 FDA reports)
SEBORRHOEIC DERMATITIS ( 28 FDA reports)
AORTIC STENOSIS ( 27 FDA reports)
HYPERTENSION ( 27 FDA reports)
MENTAL STATUS CHANGES ( 27 FDA reports)
OEDEMA PERIPHERAL ( 27 FDA reports)
OSTEOPENIA ( 27 FDA reports)
PNEUMONIA ( 27 FDA reports)
BLOOD PRESSURE INCREASED ( 26 FDA reports)
DEHYDRATION ( 26 FDA reports)
DYSGEUSIA ( 26 FDA reports)
HYPOTHYROIDISM ( 26 FDA reports)
INJURY ( 26 FDA reports)
BRONCHITIS ( 25 FDA reports)
CHEST DISCOMFORT ( 25 FDA reports)
EMOTIONAL DISTRESS ( 25 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 25 FDA reports)
HYPERCHOLESTEROLAEMIA ( 25 FDA reports)
OSTEONECROSIS OF JAW ( 25 FDA reports)
BRADYCARDIA ( 24 FDA reports)
CARDIAC MURMUR ( 24 FDA reports)
SINUS CONGESTION ( 24 FDA reports)
VENTRICULAR HYPERTROPHY ( 24 FDA reports)
AORTIC VALVE INCOMPETENCE ( 23 FDA reports)
ORAL PAIN ( 23 FDA reports)
OSTEOARTHRITIS ( 23 FDA reports)
PLATELET COUNT DECREASED ( 23 FDA reports)
VOMITING ( 23 FDA reports)
ATRIAL TACHYCARDIA ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 22 FDA reports)
BARRETT'S OESOPHAGUS ( 22 FDA reports)
BONE DISORDER ( 22 FDA reports)
CEREBROVASCULAR ACCIDENT ( 22 FDA reports)
DIVERTICULITIS ( 22 FDA reports)
GINGIVAL PAIN ( 22 FDA reports)
GINGIVAL RECESSION ( 22 FDA reports)
GINGIVAL ULCERATION ( 22 FDA reports)
HYPOACUSIS ( 22 FDA reports)
LOOSE TOOTH ( 22 FDA reports)
MULTIPLE MYELOMA ( 22 FDA reports)
RESPIRATORY FAILURE ( 22 FDA reports)
SOFT TISSUE INFLAMMATION ( 22 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 22 FDA reports)
THROMBOCYTOPENIA ( 22 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 22 FDA reports)
TOOTHACHE ( 22 FDA reports)
UMBILICAL HERNIA ( 22 FDA reports)
VISION BLURRED ( 22 FDA reports)
WOUND DEHISCENCE ( 22 FDA reports)
X-RAY ABNORMAL ( 22 FDA reports)
CONTUSION ( 21 FDA reports)
EMPHYSEMA ( 21 FDA reports)
EYE PAIN ( 21 FDA reports)
HAEMATOCRIT ABNORMAL ( 21 FDA reports)
INFLUENZA LIKE ILLNESS ( 21 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 21 FDA reports)
PALPITATIONS ( 21 FDA reports)
BACK PAIN ( 20 FDA reports)
BLOOD GLUCOSE INCREASED ( 20 FDA reports)
JOINT SWELLING ( 20 FDA reports)
RASH PRURITIC ( 20 FDA reports)
DERMAL CYST ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
PULMONARY HYPERTENSION ( 19 FDA reports)
RENAL FAILURE ( 19 FDA reports)
SPINAL OSTEOARTHRITIS ( 19 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 18 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 18 FDA reports)
RENAL FAILURE ACUTE ( 18 FDA reports)
SINUS TACHYCARDIA ( 18 FDA reports)
ANXIETY DISORDER ( 17 FDA reports)
ATELECTASIS ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 17 FDA reports)
DYSPEPSIA ( 17 FDA reports)
HYPOKALAEMIA ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
DEEP VEIN THROMBOSIS ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 16 FDA reports)
MACULAR HOLE ( 16 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 16 FDA reports)
RETINAL DETACHMENT ( 16 FDA reports)
TREMOR ( 16 FDA reports)
VITREOUS FLOATERS ( 16 FDA reports)
ACTINIC ELASTOSIS ( 15 FDA reports)
ACTINIC KERATOSIS ( 15 FDA reports)
AGGRESSION ( 15 FDA reports)
ARTHRITIS ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
HYPERSENSITIVITY ( 15 FDA reports)
POST PROCEDURAL COMPLICATION ( 15 FDA reports)
VITAMIN B12 DEFICIENCY ( 15 FDA reports)
EYE SWELLING ( 14 FDA reports)
GASTRIC ULCER ( 14 FDA reports)
HEART RATE INCREASED ( 14 FDA reports)
HYPERLIPIDAEMIA ( 14 FDA reports)
JOINT SPRAIN ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
OCULAR HYPERAEMIA ( 14 FDA reports)
ORTHOSTATIC HYPOTENSION ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
SKIN INFECTION ( 14 FDA reports)
WHEEZING ( 14 FDA reports)
ACROCHORDON ( 13 FDA reports)
COLITIS ISCHAEMIC ( 13 FDA reports)
MELANOCYTIC NAEVUS ( 13 FDA reports)
NEPHROLITHIASIS ( 13 FDA reports)
PRURITUS ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
SKIN FIBROSIS ( 13 FDA reports)
SKIN PAPILLOMA ( 13 FDA reports)
SUICIDAL IDEATION ( 13 FDA reports)
UROSEPSIS ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
VERTIGO ( 13 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
CARDIAC PACEMAKER INSERTION ( 12 FDA reports)
COGNITIVE DISORDER ( 12 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
OESOPHAGEAL SPASM ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
REFLUX OESOPHAGITIS ( 12 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 11 FDA reports)
AFFECTIVE DISORDER ( 11 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 11 FDA reports)
BONE LESION EXCISION ( 11 FDA reports)
BONE PAIN ( 11 FDA reports)
CATARACT OPERATION ( 11 FDA reports)
CHILLS ( 11 FDA reports)
DYSPHONIA ( 11 FDA reports)
DYSPLASTIC NAEVUS ( 11 FDA reports)
ENDODONTIC PROCEDURE ( 11 FDA reports)
EYE LASER SURGERY ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
LIMB OPERATION ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
PULMONARY GRANULOMA ( 11 FDA reports)
SCLERAL OPERATION ( 11 FDA reports)
STEM CELL TRANSPLANT ( 11 FDA reports)
UMBILICAL HERNIA REPAIR ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BONE LESION ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
DRUG DEPENDENCE ( 10 FDA reports)
DRY EYE ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
GENERALISED ANXIETY DISORDER ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
INFLAMMATION ( 10 FDA reports)
LACUNAR INFARCTION ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
MALAISE ( 10 FDA reports)
MYOCARDIAL ISCHAEMIA ( 10 FDA reports)
ONYCHOMYCOSIS ( 10 FDA reports)
PULMONARY FIBROSIS ( 10 FDA reports)
SCIATICA ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 10 FDA reports)
URINARY RETENTION ( 10 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
BASOPHIL COUNT INCREASED ( 9 FDA reports)
BEREAVEMENT REACTION ( 9 FDA reports)
BLEPHARITIS ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BRONCHITIS ACUTE ( 9 FDA reports)
CONVERSION DISORDER ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
HIATUS HERNIA ( 9 FDA reports)
INADEQUATE ANALGESIA ( 9 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 9 FDA reports)
JOINT EFFUSION ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LUNG INFILTRATION ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
NOCTURIA ( 9 FDA reports)
PRODUCTIVE COUGH ( 9 FDA reports)
PROSTATITIS ( 9 FDA reports)
SEASONAL ALLERGY ( 9 FDA reports)
SNORING ( 9 FDA reports)
STRESS ( 9 FDA reports)
STRESS SYMPTOMS ( 9 FDA reports)
TREATMENT NONCOMPLIANCE ( 9 FDA reports)
UNEVALUABLE EVENT ( 9 FDA reports)
URINE FLOW DECREASED ( 9 FDA reports)
ANHEDONIA ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BENIGN VASCULAR NEOPLASM ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
FEAR ( 8 FDA reports)
GANGLION ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HYPOREFLEXIA ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
NECK PAIN ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PSYCHOSOMATIC DISEASE ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
CONVULSION NEONATAL ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
POLYP ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
TALIPES ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ACUTE STRESS DISORDER ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ANAL INFLAMMATION ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
CERVICAL SPINAL STENOSIS ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CYST ( 6 FDA reports)
DISABILITY ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
EAR DISCOMFORT ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LOCAL SWELLING ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MENOPAUSAL SYMPTOMS ( 6 FDA reports)
METASTATIC NEOPLASM ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OEDEMA MUCOSAL ( 6 FDA reports)
ORTHOPNOEA ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
PARANASAL SINUS DISCOMFORT ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
THYROID DISORDER ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
VENOUS OCCLUSION ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VULVOVAGINAL DRYNESS ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DEATH ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
EYE OPERATION ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
NAIL HYPERTROPHY ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SKIN TOXICITY ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
COCCYDYNIA ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL POLYP ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
RASH ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN CYST EXCISION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TACHYCARDIA FOETAL ( 4 FDA reports)
THYMOMA ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
TORTICOLLIS ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APHONIA ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
COMPRESSION FRACTURE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MANIA ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LIFE EXPECTANCY SHORTENED ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEOARTHRITIS GENERALISED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SPINAL CLAUDICATION ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTASTHMATIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERIORBITAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)

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