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

DYSPNOEA ( 23 FDA reports)
PNEUMONIA ( 15 FDA reports)
WHEEZING ( 15 FDA reports)
BRONCHITIS ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
HYPERSENSITIVITY ( 13 FDA reports)
INFLUENZA ( 13 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 12 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 12 FDA reports)
SPUTUM DISCOLOURED ( 12 FDA reports)
PRURITUS ( 11 FDA reports)
DYSPNOEA EXERTIONAL ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
FATIGUE ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
CYTOKINE RELEASE SYNDROME ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
CHILLS ( 4 FDA reports)
DEATH ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RASH ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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