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

DYSPNOEA ( 15 FDA reports)
ASTHMA ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
PERICARDIAL EFFUSION ( 10 FDA reports)
COUGH ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
PLATELET COUNT INCREASED ( 8 FDA reports)
CONVULSION ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ARTHRITIS ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PAIN ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
DIAPHRAGMATIC DISORDER ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FALL ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MYOPERICARDITIS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCAR ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INJECTION SITE CYST ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL APLASTIC ANAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EXPOSURE TO CONTAMINATED AIR ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOEFFLER'S SYNDROME ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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