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
125713691 12571369 1 I 201607 20160715 20160719 20160719 PER US-BAYER-2016-139685 BAYER 73.00 YR E F Y 53.97000 KG 20160719 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
125713691 12571369 1 PS CLARITIN REDITABS LORATADINE 1 Oral 1 DF, QD MEBT52 20704 1 DF ORODISPERSIBLE TABLET QD
125713691 12571369 2 C BUSPIRONE BUSPIRONE HYDROCHLORIDE 1 0
125713691 12571369 3 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
125713691 12571369 4 C PAROXETINE. PAROXETINE 1 0
125713691 12571369 5 C GENTEAL MILD HYPROMELLOSE 2910 (4000 MPA.S) 1 0
125713691 12571369 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
125713691 12571369 7 C VITAMIN B12 CYANOCOBALAMIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125713691 12571369 1 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125713691 12571369 Drug ineffective
125713691 12571369 Intercepted medication error

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
125713691 12571369 1 201607 20160715 0