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
85368062 8536806 2 F 200602 20080630 20080710 20120424 PER PHEH2008US04324 NOVARTIS 27.00 YR F N 160.50000 KG 20090526 MD 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
85368062 8536806 1 PS LOTENSIN HCT 1 20033 TABLET
85368062 8536806 2 SS LOTENSIN 1 0
85368062 8536806 3 SS ALDOMET 1 U U 0 250 MG BID
85368062 8536806 5 C HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) 1 0
85368062 8536806 7 C CLARITIN (LORATADINE) 2 0
85368062 8536806 9 C TYLENOL (PARACETAMOL) 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
85368062 8536806 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
85368062 8536806 Abortion spontaneous
85368062 8536806 Evacuation of retained products of conception
85368062 8536806 Maternal exposure during pregnancy

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

Event ID CASEID RPSR COD
85368062 8536806 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
85368062 8536806 2 20031123 0
85368062 8536806 3 200510 0
85368062 8536806 3 20040723 0