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

ANOSMIA ( 28 FDA reports)
DYSPNOEA ( 23 FDA reports)
ASTHMA ( 22 FDA reports)
OFF LABEL USE ( 12 FDA reports)
MALAISE ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
AGEUSIA ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ASTHMATIC CRISIS ( 6 FDA reports)
HYPERTENSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
CATARACT ( 4 FDA reports)
COUGH ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
SWELLING ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ACNE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FALL ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use