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
126610621 12661062 1 I 20160809 20160817 20160817 EXP BR-ASTRAZENECA-2016SE87147 ASTRAZENECA 4.00 MON F Y 0.00000 20160817 OT BR BR

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
126610621 12661062 1 PS MEROPENEM. MEROPENEM 1 Intravenous (not otherwise specified) U 50706 SOLUTION FOR INJECTION
126610621 12661062 2 C VANCOMYCIN VANCOMYCIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126610621 12661062 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126610621 12661062 Chronic papillomatous dermatitis
126610621 12661062 Drug ineffective
126610621 12661062 Pyoderma gangrenosum
126610621 12661062 Scar

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

no results found

Therapies reported

no results found