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
98297393 9829739 3 F 20150429 20140120 20160714 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-19990910 BRISTOL MYERS SQUIBB 35.00 YR F Y 0.00000 20160714 OT DE DE

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
98297393 9829739 1 PS TRIAMCINOLONE ACETONIDE. TRIAMCINOLONE ACETONIDE 1 Unknown 20 MG, UNK U 12041 20 MG INJECTION
98297393 9829739 2 I RITONAVIR. RITONAVIR 1 Unknown 100 MG, BID 0 100 MG BID
98297393 9829739 3 C BUPIVACAINE. BUPIVACAINE 1 Unknown UNK UNK, QWK U 0 /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98297393 9829739 1 Lumbar spinal stenosis
98297393 9829739 2 HIV infection
98297393 9829739 3 Lumbar spinal stenosis

Outcome of event

Event ID CASEID OUTC COD
98297393 9829739 OT
98297393 9829739 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98297393 9829739 Adrenal suppression
98297393 9829739 Cushing's syndrome
98297393 9829739 Drug interaction

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
98297393 9829739 1 201206 0
98297393 9829739 2 200507 0
98297393 9829739 3 201206 0