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

PAIN ( 45 FDA reports)
CHOLECYSTITIS CHRONIC ( 30 FDA reports)
ANXIETY ( 26 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
CHOLELITHIASIS ( 24 FDA reports)
INJURY ( 24 FDA reports)
DYSPNOEA ( 23 FDA reports)
CHEST PAIN ( 22 FDA reports)
ANHEDONIA ( 19 FDA reports)
BACK PAIN ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
URINARY TRACT INFECTION ( 19 FDA reports)
HIATUS HERNIA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
ABDOMINAL PAIN UPPER ( 17 FDA reports)
DIARRHOEA ( 15 FDA reports)
DIVERTICULUM ( 15 FDA reports)
GALLBLADDER DISORDER ( 15 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
ARTHRITIS ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
FALL ( 14 FDA reports)
IRON DEFICIENCY ANAEMIA ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
RIB FRACTURE ( 14 FDA reports)
BONE PAIN ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
HAEMATURIA ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
OSTEONECROSIS ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
BLADDER NEOPLASM ( 12 FDA reports)
BONE DISORDER ( 12 FDA reports)
BONE LESION ( 12 FDA reports)
BREAST CANCER RECURRENT ( 12 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 12 FDA reports)
BRONCHITIS ( 12 FDA reports)
BRUXISM ( 12 FDA reports)
CONTUSION ( 12 FDA reports)
DENTAL CARIES ( 12 FDA reports)
DENTAL PLAQUE ( 12 FDA reports)
DEVICE RELATED INFECTION ( 12 FDA reports)
DIPLOPIA ( 12 FDA reports)
DISABILITY ( 12 FDA reports)
DYSGEUSIA ( 12 FDA reports)
EMPHYSEMA ( 12 FDA reports)
GINGIVAL EROSION ( 12 FDA reports)
GINGIVAL OEDEMA ( 12 FDA reports)
HOT FLUSH ( 12 FDA reports)
HYDRONEPHROSIS ( 12 FDA reports)
INFECTION ( 12 FDA reports)
KYPHOSIS ( 12 FDA reports)
LIPOMA ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
ORAL PAIN ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 12 FDA reports)
PERIODONTAL DISEASE ( 12 FDA reports)
RENAL CYST ( 12 FDA reports)
ROAD TRAFFIC ACCIDENT ( 12 FDA reports)
SCOLIOSIS ( 12 FDA reports)
SPINAL FRACTURE ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
TOOTH ABSCESS ( 12 FDA reports)
TOOTH DEPOSIT ( 12 FDA reports)
TOOTH FRACTURE ( 12 FDA reports)
BURSITIS ( 11 FDA reports)
DYSPEPSIA ( 11 FDA reports)
ILEUS ( 11 FDA reports)
MENISCUS LESION ( 11 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
CHILLS ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
METASTASES TO SPINE ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
COUGH ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
ATELECTASIS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
SINUS CONGESTION ( 5 FDA reports)
STRESS ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
VERTEBRAL WEDGING ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACNE ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
FEAR ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLISTER ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAPNOCYTOPHAGA INFECTION ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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