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
127690731 12769073 1 I 20160904 20160906 20160921 20160921 PER US-BAYER-2016-173583 BAYER 82.00 YR E F Y 74.83000 KG 20160921 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
127690731 12769073 1 PS CLARITIN LORATADINE 1 Oral 1 DF, TWICE N CVM06KY 19658 1 DF TABLET
127690731 12769073 2 SS CLARITIN LORATADINE 1 N 19658 TABLET
127690731 12769073 3 C WARFARIN WARFARIN 1 UNK 0
127690731 12769073 4 C LABETALOL LABETALOLLABETALOL HYDROCHLORIDE 1 UNK 0
127690731 12769073 5 C VITAMIN D CHOLECALCIFEROL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127690731 12769073 1 Hypersensitivity
127690731 12769073 2 Nasopharyngitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127690731 12769073 Drug ineffective
127690731 12769073 Headache
127690731 12769073 Product use issue
127690731 12769073 Rhinorrhoea

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
127690731 12769073 1 20160904 20160904 0