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
127453511 12745351 1 I 20160829 0 20160914 20160914 DIR US-FDA-350609 FDA-CTU 58.00 YR F N 0.00000 20160914 Y LW 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
127453511 12745351 1 PS LIDOCAINE. LIDOCAINE 1 OTHER STRENGTH:;OTHER DOSE:;OTHER FREQUENCY:ONCE;OTHER ROUTE:INJECTION INTO BURSA D U 63-460-DK 20180301 0 2 ML
127453511 12745351 2 SS BUPIVACAINE. BUPIVACAINE 1 OTHER STRENGTH:;OTHER DOSE:;OTHER FREQUENCY:ONCE;OTHER ROUTE:INJECTION INTO BURSA D D 63-195-DK 20180301 0 2 ML

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127453511 12745351 1 Bursitis
127453511 12745351 2 Bursitis

Outcome of event

Event ID CASEID OUTC COD
127453511 12745351 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127453511 12745351 Pain in extremity
127453511 12745351 Product quality issue
127453511 12745351 Staphylococcal infection

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
127453511 12745351 1 20160829 0
127453511 12745351 2 20160829 0