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
125393501 12539350 1 I 20160624 20160708 20160708 PER US-BAYER-2016-126064 BAYER 86.00 YR E F Y 45.81000 KG 20160708 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
125393501 12539350 1 PS CLARITIN LORATADINE 1 UNK CVM03EK 19658 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125393501 12539350 1 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125393501 12539350 Cough
125393501 12539350 Dizziness
125393501 12539350 Movement disorder
125393501 12539350 Product use issue

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

no results found

Therapies reported

no results found