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
125184413 12518441 3 F 201606 20160615 20160630 20160701 EXP AU-SAOL THERAPEUTICS-2016SAO00009 SAOL THERAPEUTICS 66.63 YR M Y 0.00000 20160630 CN COUNTRY NOT SPECIFIED AU

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
125184413 12518441 1 PS LIORESAL BACLOFEN 1 Intrathecal 159.76 ?G, UNK U U S0006 20075 159.76 UG
125184413 12518441 2 SS LIORESAL BACLOFEN 1 Intrathecal 219.92 ?G, UNK U U S0006 20075 219.92 UG
125184413 12518441 3 SS MORPHINE MORPHINE 1 Intrathecal 116.21 ?G, UNK 0 116.21 UG
125184413 12518441 4 SS MORPHINE MORPHINE 1 Intrathecal 159.95 UNK, UNK 0 159.95 UG
125184413 12518441 5 SS SALINE SODIUM CHLORIDE 1 0.174 MG, UNK 0 .174 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125184413 12518441 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125184413 12518441 Device failure
125184413 12518441 Fall

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
125184413 12518441 1 20160613 0
125184413 12518441 2 20160613 0
125184413 12518441 3 20160613 0
125184413 12518441 4 20160613 0