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

DYSPNOEA ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
PULMONARY CONGESTION ( 16 FDA reports)
BRONCHITIS ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
ASTHMA ( 12 FDA reports)
COUGH ( 12 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
POLYP ( 11 FDA reports)
RHINORRHOEA ( 11 FDA reports)
OTITIS MEDIA ( 10 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 10 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
NASAL CONGESTION ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
PRODUCTIVE COUGH ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
SINUS CONGESTION ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
ENDOPHTHALMITIS ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
INSULIN RESISTANCE ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
PAIN ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 7 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 6 FDA reports)
DEATH ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
SUPERINFECTION ( 6 FDA reports)
JOINT SWELLING ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MALAISE ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PSEUDOENDOPHTHALMITIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E DECREASED ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CYSTIC FIBROSIS LUNG ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANTERIOR CHAMBER FLARE ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AURAL POLYP ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHORIORETINAL ATROPHY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORDER OF GLOBE ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM OF ORBIT ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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