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
126472451 12647245 1 I 20160808 0 20160811 20160811 DIR 38.00 YR F N 153.00000 LBS 20160809 Y 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
126472451 12647245 1 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 1 TABLET(S) AT BEDTIME TAKEN BY MOUTH N Y 439428 20161031 0 1 DF COATED TABLET HS
126472451 12647245 3 C VALACYCLAVIR 2 0
126472451 12647245 5 C ALEVE NAPROXEN SODIUM 1 0
126472451 12647245 7 C IBUPROFEN. IBUPROFEN 1 0
126472451 12647245 9 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 0
126472451 12647245 11 C PEPCID FAMOTIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126472451 12647245 1 Multiple allergies

Outcome of event

Event ID CASEID OUTC COD
126472451 12647245 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126472451 12647245 Discomfort
126472451 12647245 Drug withdrawal syndrome
126472451 12647245 Feeling abnormal
126472451 12647245 Pruritus
126472451 12647245 Rash
126472451 12647245 Urticaria

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
126472451 12647245 1 6 MON