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

INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
COUGH ( 11 FDA reports)
ARTHRALGIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
SWELLING ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FAMILIAL MEDITERRANEAN FEVER ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
TONGUE ERUPTION ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
IMMOBILISATION PROLONGED ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)

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