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

ANAPHYLACTIC REACTION ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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