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

PAIN ( 80 FDA reports)
DRUG INTERACTION ( 77 FDA reports)
PNEUMONIA ( 71 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 68 FDA reports)
PULMONARY EMBOLISM ( 65 FDA reports)
MYOSITIS ( 64 FDA reports)
PLEURAL EFFUSION ( 64 FDA reports)
ATRIAL FIBRILLATION ( 62 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 61 FDA reports)
OEDEMA PERIPHERAL ( 60 FDA reports)
DYSPNOEA ( 55 FDA reports)
PERICARDIAL EFFUSION ( 55 FDA reports)
ASTHENIA ( 54 FDA reports)
HYPOKALAEMIA ( 45 FDA reports)
ANXIETY ( 42 FDA reports)
RASH ( 42 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 41 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 40 FDA reports)
FLUID OVERLOAD ( 39 FDA reports)
MYALGIA ( 39 FDA reports)
INJURY ( 38 FDA reports)
HYPOTENSION ( 37 FDA reports)
RENAL FAILURE ACUTE ( 36 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 34 FDA reports)
CARDIAC ARREST ( 33 FDA reports)
ERYTHEMA ( 33 FDA reports)
INFECTION ( 33 FDA reports)
MYOPATHY ( 32 FDA reports)
HYPERTENSION ( 31 FDA reports)
HYPOKINESIA ( 31 FDA reports)
OEDEMA ( 31 FDA reports)
ABDOMINAL PAIN ( 29 FDA reports)
BRADYCARDIA ( 29 FDA reports)
TACHYCARDIA ( 29 FDA reports)
DEPRESSION ( 28 FDA reports)
PRURITUS ( 28 FDA reports)
RENAL FAILURE ( 28 FDA reports)
BRONCHOSPASM ( 27 FDA reports)
CARDIOMEGALY ( 27 FDA reports)
ANHEDONIA ( 26 FDA reports)
ARRHYTHMIA ( 26 FDA reports)
HAEMOGLOBIN DECREASED ( 26 FDA reports)
PAIN IN EXTREMITY ( 26 FDA reports)
DIZZINESS ( 25 FDA reports)
FATIGUE ( 25 FDA reports)
NAUSEA ( 25 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 25 FDA reports)
EMOTIONAL DISTRESS ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 22 FDA reports)
FALL ( 22 FDA reports)
PALPITATIONS ( 22 FDA reports)
URTICARIA ( 22 FDA reports)
ARTHRITIS ( 21 FDA reports)
BACK PAIN ( 21 FDA reports)
BLOOD CREATININE INCREASED ( 21 FDA reports)
CARDIAC MURMUR ( 21 FDA reports)
HEPATIC STEATOSIS ( 21 FDA reports)
HYPERLIPIDAEMIA ( 21 FDA reports)
HYPERSENSITIVITY ( 21 FDA reports)
STEVENS-JOHNSON SYNDROME ( 21 FDA reports)
ASTHMA ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 20 FDA reports)
JOINT SWELLING ( 20 FDA reports)
OSTEOPENIA ( 20 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 20 FDA reports)
UNEVALUABLE EVENT ( 20 FDA reports)
BLISTER ( 19 FDA reports)
BRONCHITIS ( 19 FDA reports)
CONTUSION ( 19 FDA reports)
DRY SKIN ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
SPINAL OSTEOARTHRITIS ( 19 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 18 FDA reports)
CELLULITIS ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 18 FDA reports)
CONSTIPATION ( 18 FDA reports)
DIVERTICULUM INTESTINAL ( 18 FDA reports)
DRUG INEFFECTIVE ( 18 FDA reports)
DYSPNOEA EXERTIONAL ( 18 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 18 FDA reports)
HAEMORRHOIDS ( 18 FDA reports)
NECK PAIN ( 18 FDA reports)
OSTEOARTHRITIS ( 18 FDA reports)
PETECHIAE ( 18 FDA reports)
RASH MACULO-PAPULAR ( 18 FDA reports)
SWELLING FACE ( 18 FDA reports)
CHRONIC SINUSITIS ( 17 FDA reports)
DEEP VEIN THROMBOSIS ( 17 FDA reports)
ECZEMA ( 17 FDA reports)
GOITRE ( 17 FDA reports)
INSOMNIA ( 17 FDA reports)
LYMPHOEDEMA ( 17 FDA reports)
METASTASES TO BONE ( 17 FDA reports)
OSTEOPOROSIS ( 17 FDA reports)
RASH GENERALISED ( 17 FDA reports)
RASH PRURITIC ( 17 FDA reports)
SCAB ( 17 FDA reports)
SKIN DISORDER ( 17 FDA reports)
SKIN TIGHTNESS ( 17 FDA reports)
SLEEP APNOEA SYNDROME ( 17 FDA reports)
ACETABULUM FRACTURE ( 16 FDA reports)
BONE LESION ( 16 FDA reports)
CARPAL TUNNEL SYNDROME ( 16 FDA reports)
COUGH ( 16 FDA reports)
DISABILITY ( 16 FDA reports)
FEAR ( 16 FDA reports)
GINGIVAL ERYTHEMA ( 16 FDA reports)
GINGIVAL PAIN ( 16 FDA reports)
GROIN PAIN ( 16 FDA reports)
HAEMATOMA ( 16 FDA reports)
HEAD INJURY ( 16 FDA reports)
KIDNEY INFECTION ( 16 FDA reports)
MUMPS ( 16 FDA reports)
NECK INJURY ( 16 FDA reports)
NEPHROLITHIASIS ( 16 FDA reports)
ORAL INFECTION ( 16 FDA reports)
OSTEITIS ( 16 FDA reports)
OSTEONECROSIS OF JAW ( 16 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 16 FDA reports)
POLLAKIURIA ( 16 FDA reports)
RECTAL POLYP ( 16 FDA reports)
RUBELLA ( 16 FDA reports)
SCARLET FEVER ( 16 FDA reports)
SCOLIOSIS ( 16 FDA reports)
SEASONAL ALLERGY ( 16 FDA reports)
SKIN EXFOLIATION ( 16 FDA reports)
TENDONITIS ( 16 FDA reports)
VENTRICULAR TACHYCARDIA ( 16 FDA reports)
VITAMIN D DECREASED ( 16 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 15 FDA reports)
CANDIDIASIS ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
DYSPEPSIA ( 15 FDA reports)
HEART RATE INCREASED ( 15 FDA reports)
HYPERKALAEMIA ( 15 FDA reports)
INFUSION RELATED REACTION ( 15 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 15 FDA reports)
LIGAMENT INJURY ( 15 FDA reports)
OBESITY ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
SWELLING ( 15 FDA reports)
TOOTHACHE ( 15 FDA reports)
VOMITING ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
EXOSTOSIS ( 14 FDA reports)
FACET JOINT SYNDROME ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
HYPERMETABOLISM ( 14 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
MOBILITY DECREASED ( 14 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 14 FDA reports)
NEOPLASM MALIGNANT ( 14 FDA reports)
NEOPLASM PROGRESSION ( 14 FDA reports)
NODULE ( 14 FDA reports)
SKIN HYPERTROPHY ( 14 FDA reports)
SKIN INDURATION ( 14 FDA reports)
WHEEZING ( 14 FDA reports)
CHEST PAIN ( 13 FDA reports)
CIRCULATORY COLLAPSE ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
SCAR ( 13 FDA reports)
SKIN HYPERPIGMENTATION ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
DEFORMITY ( 12 FDA reports)
FIBROSIS ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
JOINT STIFFNESS ( 12 FDA reports)
MITRAL VALVE PROLAPSE ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
MUSCLE SPASMS ( 12 FDA reports)
PAIN OF SKIN ( 12 FDA reports)
SKIN FIBROSIS ( 12 FDA reports)
SKIN PLAQUE ( 12 FDA reports)
STRESS ( 12 FDA reports)
ARTERIOSPASM CORONARY ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
MALAISE ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PULMONARY FIBROSIS ( 11 FDA reports)
RENAL INJURY ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
SINUS BRADYCARDIA ( 11 FDA reports)
TENOSYNOVITIS STENOSANS ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
BREATH SOUNDS ABNORMAL ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
FACIAL PAIN ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
TACHYPNOEA ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
APNOEA ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
PROCEDURAL COMPLICATION ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
TOOTH INFECTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 7 FDA reports)
DEATH ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DILATATION ATRIAL ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 7 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PALLOR ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
TREMOR ( 7 FDA reports)
VENTRICULAR FIBRILLATION ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
BONE LOSS ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
VENTRICULAR HYPERTROPHY ( 6 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FRACTURE MALUNION ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 5 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANURIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEVICE OCCLUSION ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PRESBYACUSIS ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
APATHY ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATARACT ( 3 FDA reports)
COELIAC ARTERY OCCLUSION ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYRINGE ISSUE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VEIN WALL HYPERTROPHY ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
UMBILICAL MALFORMATION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR PRE-EXCITATION ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use