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
123785242 12378524 2 F 201602 20160713 20160517 20160715 EXP US-BAYER-2016-092657 BAYER 72.00 YR E M Y 106.58000 KG 20160715 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
123785242 12378524 1 PS CLARITIN REDITABS LORATADINE 1 Oral 1 DF, QD Y MEBT9 20704 1 DF ORODISPERSIBLE TABLET QD
123785242 12378524 2 SS CLARITIN LORATADINE 1 Oral UNK NOT PROVIDED 0 TABLET
123785242 12378524 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123785242 12378524 1 Seasonal allergy
123785242 12378524 2 Seasonal allergy

Outcome of event

Event ID CASEID OUTC COD
123785242 12378524 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123785242 12378524 Drug effect delayed
123785242 12378524 Heart rate increased
123785242 12378524 Hypertension
123785242 12378524 Product use issue
123785242 12378524 Pulse absent
123785242 12378524 Therapeutic response unexpected
123785242 12378524 Tremor

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
123785242 12378524 1 201602 201604 0
123785242 12378524 2 201602 201602 0