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

DYSPNOEA ( 18 FDA reports)
ASTHMA ( 16 FDA reports)
ARTHRALGIA ( 12 FDA reports)
BACK PAIN ( 11 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
EPIDURAL LIPOMATOSIS ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
MALAISE ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
GINGIVAL HYPERPLASIA ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
ORAL MUCOSA EROSION ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CHOKING ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
JOINT CREPITATION ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
RASH ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
ASTHMATIC CRISIS ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
PRIMARY HYPOGONADISM ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INJURY ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
THIRST ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use