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
125644641 12564464 1 I 20151203 20151204 20160718 20160718 EXP US-CIPLA LTD.-2016US07107 CIPLA 0.00 Y 0.00000 20160718 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
125644641 12564464 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Oral 4 MG, QD (2 TABLETS) UNKNOWN 90935 4 MG TABLET
125644641 12564464 2 I PROTONIX PANTOPRAZOLE SODIUM 1 Oral 40 MG, DAILY U U 0 40 MG
125644641 12564464 3 C ATENOLOL. ATENOLOL 1 Oral 50 MG, QD U U 0 50 MG
125644641 12564464 4 C Hydrochlorthiazide HYDROCHLOROTHIAZIDE 1 Oral 25 MG, DAILY U U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125644641 12564464 3 Hypertension
125644641 12564464 4 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125644641 12564464 Drug interaction
125644641 12564464 International normalised ratio increased

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
125644641 12564464 1 20151109 0
125644641 12564464 2 20151103 0