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
126779021 12677902 1 I 201508 20160414 20160823 20160823 PER US-TARO-2016TAR00342 TARO 70.48 YR F Y 86.17000 KG 20160811 CN 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
126779021 12677902 1 PS WARFARIN SODIUM TABLETS USP 5MG WARFARIN SODIUM 1 Oral 5 MG, 3X/WEEK 40301 5 MG TABLET TIW
126779021 12677902 2 SS WARFARIN SODIUM TABLETS USP 5MG WARFARIN SODIUM 1 Oral 2.5 MG, 4X/WEEK 40301 2.5 MG TABLET
126779021 12677902 3 SS WARFARIN SODIUM TABLETS USP 5MG WARFARIN SODIUM 1 40301 TABLET
126779021 12677902 4 C AMIODARONE AMIODARONE 1 200 MG, 1X/DAY 0 200 MG QD
126779021 12677902 5 C AMLODIPINE AMLODIPINE BESYLATE 1 20 MG, 1X/DAY 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126779021 12677902 1 Protein S deficiency
126779021 12677902 2 Deep vein thrombosis
126779021 12677902 3 Atrial fibrillation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126779021 12677902 Hypersensitivity

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

no results found

Therapies reported

no results found