The Safety Rates Drug Report

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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
125645181 12564518 1 I 20160330 20160718 20160718 EXP US-CIPLA LTD.-2016US07119 CIPLA 0.00 Y 0.00000 20160718 PH 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
125645181 12564518 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Oral 1 MG, UNK 11510645 90935 1 MG TABLET
125645181 12564518 2 SS WARFARIN SODIUM. WARFARIN SODIUM 1 Oral 2 MG, QD 11511960 90935 2 MG TABLET
125645181 12564518 3 SS WARFARIN SODIUM. WARFARIN SODIUM 1 Oral 4 MG, BID 11510740 90935 4 MG TABLET
125645181 12564518 4 C TRICOR FENOFIBRATE 1 Unknown 145 MG, QD U U 0 145 MG TABLET
125645181 12564518 5 C ATENOLOL. ATENOLOL 1 Unknown 25 MG, AT NIGHT U U 0 25 MG TABLET
125645181 12564518 6 C LOSARTAN. LOSARTAN 1 Unknown 25 MG, UNK U U 0 25 MG TABLET
125645181 12564518 7 C Pantoprazole PANTOPRAZOLE SODIUM 1 Unknown 40 MG, UNK U U 0 40 MG TABLET

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125645181 12564518 International normalised ratio decreased
125645181 12564518 Product colour issue

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

no results found

Therapies reported

no results found