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
126852691 12685269 1 I 20160817 20160825 20160825 EXP PHHY2016US113523 SANDOZ 19.00 YR M Y 72.56000 KG 20160825 OT 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
126852691 12685269 1 PS DOXYCYCLINE. DOXYCYCLINE 1 Oral 100 MG, BID 65353 100 MG BID
126852691 12685269 2 C PROBIOTIC COMPLEX 2 Unknown 20 BILLION CFU U 0
126852691 12685269 3 C SACCHAROMYCES BOULARDII SACCHAROMYCES CEREVISIAE 1 Unknown 500 MG U 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126852691 12685269 1 Lyme disease
126852691 12685269 2 Lyme disease
126852691 12685269 3 Lyme disease

Outcome of event

Event ID CASEID OUTC COD
126852691 12685269 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126852691 12685269 Jarisch-Herxheimer reaction

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

no results found

Therapies reported

no results found