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
125710951 12571095 1 I 201603 20160712 20160719 20160719 EXP US-TAKEDA-2016TUS012328 TAKEDA 84.43 YR M Y 72.56000 KG 20160719 MD US US

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
125710951 12571095 1 PS COLCHICINE. COLCHICINE 1 Oral UNK UNK, BID Y 22352 TABLET BID
125710951 12571095 2 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral UNK U 0
125710951 12571095 3 C FLOMAX TAMSULOSIN HYDROCHLORIDE 1 Oral UNK U 0
125710951 12571095 4 C LASIX FUROSEMIDE 1 Oral UNK U 0
125710951 12571095 5 C ASPIRIN /00002701/ ASPIRIN 1 Oral 81 MG, QD U 0 81 MG QD
125710951 12571095 6 C ATORVASTATIN ATORVASTATIN 1 Oral UNK U 0
125710951 12571095 7 C AMIODARONE AMIODARONE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125710951 12571095 1 Pericarditis
125710951 12571095 2 Anticoagulant therapy
125710951 12571095 3 Prostatic disorder
125710951 12571095 4 Dysuria
125710951 12571095 6 Blood cholesterol increased
125710951 12571095 7 Heart rate irregular

Outcome of event

Event ID CASEID OUTC COD
125710951 12571095 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125710951 12571095 Off label use
125710951 12571095 Pleural effusion
125710951 12571095 Wrong technique in product usage process

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125710951 12571095 1 201603 201604 0