The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127073811 12707381 1 I 20160627 20160901 20160901 EXP CH-SA-2016SA120205 AVENTIS VALENTI A, CASUTT A, KOUTSOKERA A, NOETZLI J, PERENTES JY, KRUEGER T, ET AL. LATE MAJOR HEMOPTYSIS AFTER LUNG VOLUME REDUCTION WITH COILS INDUCED BY DUAL ANTIAGGREGATION THERAPY. ANN THORAC SURG 2016 FEB 01;101(2):E49-50. AVAILABLE FROM: HTTP://DX.DOI.ORG/10.1016/J.ATHORACSUR.2015.06.045. 55.00 YR A M Y 0.00000 20160901 MD CH CH

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127073811 12707381 1 PS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown Y N UNKNOWN 20839 75 MG QD
127073811 12707381 2 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown Y N UNKNOWN 20839 75 MG QD
127073811 12707381 3 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown Y N UNKNOWN 20839
127073811 12707381 4 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown Y N UNKNOWN 20839
127073811 12707381 5 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown Y N UNKNOWN 20839
127073811 12707381 6 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown Y N UNKNOWN 20839
127073811 12707381 7 SS ASPIRIN. ASPIRIN 1 Unknown Y UNKNOWN 0 100 MG QD
127073811 12707381 8 SS ASPIRIN. ASPIRIN 1 Unknown Y UNKNOWN 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127073811 12707381 1 Anticoagulant therapy
127073811 12707381 2 Arthralgia
127073811 12707381 3 Anticoagulant therapy
127073811 12707381 4 Arthralgia
127073811 12707381 5 Anticoagulant therapy
127073811 12707381 6 Arthralgia
127073811 12707381 7 Anticoagulant therapy
127073811 12707381 8 Peripheral arterial occlusive disease

Outcome of event

Event ID CASEID OUTC COD
127073811 12707381 LT
127073811 12707381 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127073811 12707381 Accidental exposure to product
127073811 12707381 Bronchoscopy abnormal
127073811 12707381 Haemoptysis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found