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

DYSPNOEA ( 35 FDA reports)
PAIN ( 35 FDA reports)
CHEST PAIN ( 28 FDA reports)
HYPERTENSION ( 28 FDA reports)
INJURY ( 28 FDA reports)
ANXIETY ( 25 FDA reports)
OEDEMA PERIPHERAL ( 24 FDA reports)
HEADACHE ( 23 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 21 FDA reports)
DEEP VEIN THROMBOSIS ( 21 FDA reports)
DIARRHOEA ( 21 FDA reports)
ASTHENIA ( 19 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
TYPE 2 DIABETES MELLITUS ( 19 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 17 FDA reports)
COUGH ( 17 FDA reports)
DENTAL CARIES ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
FALL ( 17 FDA reports)
ATRIAL SEPTAL DEFECT ( 16 FDA reports)
CARDIOMEGALY ( 16 FDA reports)
DIABETES MELLITUS ( 16 FDA reports)
FATIGUE ( 16 FDA reports)
VOMITING ( 16 FDA reports)
BRADYCARDIA ( 15 FDA reports)
DEPRESSION ( 15 FDA reports)
ANGINA PECTORIS ( 14 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
PULMONARY HYPERTENSION ( 14 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
URINARY TRACT INFECTION ( 14 FDA reports)
AMENORRHOEA ( 13 FDA reports)
CYANOSIS ( 13 FDA reports)
DIZZINESS ( 13 FDA reports)
FAILURE TO THRIVE ( 13 FDA reports)
HEART VALVE INCOMPETENCE ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 13 FDA reports)
RESPIRATORY DEPTH INCREASED ( 13 FDA reports)
TOOTH INJURY ( 13 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 13 FDA reports)
AORTIC VALVE INCOMPETENCE ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
MIGRAINE ( 12 FDA reports)
NECK INJURY ( 12 FDA reports)
PULMONARY VALVE STENOSIS ( 12 FDA reports)
RESPIRATION ABNORMAL ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
SUICIDE ATTEMPT ( 12 FDA reports)
TACHYPNOEA ( 12 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 12 FDA reports)
BRONCHITIS ( 11 FDA reports)
EAR INFECTION ( 11 FDA reports)
HYPERCOAGULATION ( 11 FDA reports)
NEUROPATHY PERIPHERAL ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
PERIPHERAL COLDNESS ( 11 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
TREMOR ( 11 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
CHOLECYSTITIS CHRONIC ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
HYPOACUSIS ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
AMNESIA ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 8 FDA reports)
SCLERAL HAEMORRHAGE ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CYSTITIS HAEMORRHAGIC ( 7 FDA reports)
DIABETIC RETINOPATHY ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
NEPHROLITHIASIS ( 7 FDA reports)
OBESITY ( 7 FDA reports)
OSTEONECROSIS OF JAW ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ABNORMAL SENSATION IN EYE ( 6 FDA reports)
BACK INJURY ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PATHOLOGICAL GAMBLING ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VITREOUS DETACHMENT ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ANHEDONIA ( 5 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
CALCULUS URETERIC ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
COSTOCHONDRITIS ( 5 FDA reports)
DEATH ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SCAR ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BACTERIURIA ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BONE EROSION ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BONE SWELLING ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CRYING ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
EXTRASKELETAL OSSIFICATION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MASS ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
RASH ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VAGINAL CYST ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ADNEXA UTERI MASS ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
ALLERGIC PHARYNGITIS ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BREAST HAEMATOMA ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANISOMETROPIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTISM ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELAYED FONTANELLE CLOSURE ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
ECTOPIC KIDNEY ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC VOLVULUS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MICROPENIS ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
STARING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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