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

NAUSEA ( 46 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 36 FDA reports)
DIZZINESS ( 34 FDA reports)
FATIGUE ( 31 FDA reports)
DRUG INEFFECTIVE ( 30 FDA reports)
DYSPNOEA ( 26 FDA reports)
DYSPEPSIA ( 25 FDA reports)
VOMITING ( 23 FDA reports)
SOMNOLENCE ( 22 FDA reports)
ASTHENIA ( 20 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
COUGH ( 19 FDA reports)
MALAISE ( 19 FDA reports)
CONVULSION ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
CHEST PAIN ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
WEIGHT INCREASED ( 17 FDA reports)
ANXIETY ( 15 FDA reports)
INJURY ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
LIVER DISORDER ( 14 FDA reports)
PAIN ( 14 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
MUSCLE SPASMS ( 13 FDA reports)
RESPIRATORY DISTRESS ( 13 FDA reports)
TREMOR ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
ARTHRITIS ( 12 FDA reports)
ATRIAL SEPTAL DEFECT ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
FLATULENCE ( 12 FDA reports)
OSTEOPOROSIS ( 12 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 12 FDA reports)
SINUSITIS ( 12 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 12 FDA reports)
VISION BLURRED ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
NERVE INJURY ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
ANHEDONIA ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
BACK PAIN ( 10 FDA reports)
HYPOGLYCAEMIA ( 10 FDA reports)
IRRITABLE BOWEL SYNDROME ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ANAEMIA ( 9 FDA reports)
ARTHRALGIA ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
MIGRAINE ( 9 FDA reports)
MUSCLE TWITCHING ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
GALLBLADDER DISORDER ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
HERPES VIRUS INFECTION ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
PEPTIC ULCER ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
POLYP ( 8 FDA reports)
RASH ( 8 FDA reports)
BONE PAIN ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GENERALISED OEDEMA ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CARDIAC MURMUR ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
ERUCTATION ( 5 FDA reports)
FALL ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GINGIVAL EROSION ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
KNEE ARTHROPLASTY ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
AGITATION ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DEATH ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEAR ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERTROPHIC SCAR ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
KELOID SCAR ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
PECTUS CARINATUM ( 4 FDA reports)
PICKWICKIAN SYNDROME ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POSTNASAL DRIP ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CRYING ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
NEONATAL RESPIRATORY ARREST ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RALES ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TRACHEAL INJURY ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATELECTASIS NEONATAL ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AURA ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYST ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL OEDEMA ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL TACHYCARDIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REGRESSIVE BEHAVIOUR ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
STOMATITIS HAEMORRHAGIC ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CALCIUM INTOXICATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use