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

DYSPNOEA ( 188 FDA reports)
ASTHMA ( 181 FDA reports)
COUGH ( 126 FDA reports)
NASOPHARYNGITIS ( 111 FDA reports)
FATIGUE ( 110 FDA reports)
PNEUMONIA ( 91 FDA reports)
WHEEZING ( 86 FDA reports)
HEADACHE ( 85 FDA reports)
DIZZINESS ( 80 FDA reports)
BLOOD PRESSURE INCREASED ( 74 FDA reports)
CHEST DISCOMFORT ( 61 FDA reports)
PRODUCTIVE COUGH ( 59 FDA reports)
ASTHENIA ( 55 FDA reports)
BRONCHITIS ( 52 FDA reports)
MALAISE ( 52 FDA reports)
CHEST PAIN ( 48 FDA reports)
BLOOD PRESSURE DECREASED ( 47 FDA reports)
HYPERSENSITIVITY ( 47 FDA reports)
SINUSITIS ( 46 FDA reports)
PAIN ( 41 FDA reports)
INFLUENZA ( 40 FDA reports)
DYSPHONIA ( 37 FDA reports)
FALL ( 37 FDA reports)
HEART RATE INCREASED ( 37 FDA reports)
MUSCLE SPASMS ( 36 FDA reports)
PRURITUS ( 33 FDA reports)
NAUSEA ( 32 FDA reports)
OROPHARYNGEAL PAIN ( 32 FDA reports)
PALPITATIONS ( 31 FDA reports)
SPUTUM DISCOLOURED ( 31 FDA reports)
ANAPHYLACTIC REACTION ( 30 FDA reports)
ATRIAL FIBRILLATION ( 30 FDA reports)
LUNG INFECTION ( 30 FDA reports)
PARAESTHESIA ( 30 FDA reports)
NASAL CONGESTION ( 29 FDA reports)
THROAT TIGHTNESS ( 29 FDA reports)
OEDEMA PERIPHERAL ( 28 FDA reports)
TREMOR ( 28 FDA reports)
MYOCARDIAL INFARCTION ( 27 FDA reports)
DRUG INEFFECTIVE ( 26 FDA reports)
PULMONARY CONGESTION ( 26 FDA reports)
ARTHRALGIA ( 25 FDA reports)
PYREXIA ( 25 FDA reports)
ANXIETY ( 24 FDA reports)
THROAT IRRITATION ( 24 FDA reports)
PULMONARY MASS ( 23 FDA reports)
RASH ( 23 FDA reports)
VOMITING ( 22 FDA reports)
WEIGHT DECREASED ( 21 FDA reports)
DRUG ERUPTION ( 20 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
URTICARIA ( 20 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
ALOPECIA ( 17 FDA reports)
BALANCE DISORDER ( 17 FDA reports)
BODY TEMPERATURE DECREASED ( 17 FDA reports)
HAEMOPTYSIS ( 17 FDA reports)
HYPOAESTHESIA ( 17 FDA reports)
MYALGIA ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
FLUSHING ( 16 FDA reports)
MIGRAINE ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
STRESS ( 15 FDA reports)
SWELLING FACE ( 15 FDA reports)
VIRAL INFECTION ( 15 FDA reports)
ABDOMINAL DISCOMFORT ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
HYPOAESTHESIA ORAL ( 12 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 12 FDA reports)
RHINORRHOEA ( 12 FDA reports)
SENSATION OF FOREIGN BODY ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
SLEEP DISORDER ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
BACK PAIN ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
HEARING IMPAIRED ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
BONE PAIN ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
CHOKING ( 10 FDA reports)
ECCHYMOSIS ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
PALLOR ( 10 FDA reports)
PHOTOPHOBIA ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
ECZEMA ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
PHARYNGEAL OEDEMA ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
BRONCHIECTASIS ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
GLOSSODYNIA ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
JOINT SWELLING ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
RASH PRURITIC ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
RIB FRACTURE ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
EXTRASYSTOLES ( 7 FDA reports)
FOOT FRACTURE ( 7 FDA reports)
INFECTION ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
BLADDER DISORDER ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
DEATH ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
NASAL OPERATION ( 6 FDA reports)
NASAL POLYPS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PNEUMONIA MYCOPLASMAL ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SNEEZING ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
UTERINE SPASM ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANKLE FRACTURE ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHITIS BACTERIAL ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DEVICE MALFUNCTION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GINGIVAL INFECTION ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INCREASED BRONCHIAL SECRETION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
JOINT CREPITATION ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
POLYHYDRAMNIOS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
REFLUX GASTRITIS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
AGITATION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DAYDREAMING ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INFUSION SITE URTICARIA ( 4 FDA reports)
INJECTION SITE PRURITUS ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 4 FDA reports)
POLYDACTYLY ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
PULMONARY SEQUESTRATION ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
ULCER ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ABSCESS OF EYELID ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CYSTIC FIBROSIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PERINEAL ABSCESS ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AURAL POLYP ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHLAMYDIA TEST POSITIVE ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFANTILE ASTHMA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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