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
127182661 12718266 1 I 20160822 20160906 20160906 EXP US-SAOL THERAPEUTICS-2016SAO00544 SAOL THERAPEUTICS 0.00 M Y 0.00000 20160906 MD 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
127182661 12718266 1 PS COMPOUNDED BACLOFEN BACLOFEN 1 Intrathecal UNK ?G, DAY U U 20075 INJECTION QD
127182661 12718266 2 SS COMPOUNDED BACLOFEN BACLOFEN 1 U U 20075 INJECTION
127182661 12718266 3 SS FENTANYL. FENTANYL 1 Intrathecal UNK ?G, DAY U 0 QD
127182661 12718266 4 SS BUPIVACAINE. BUPIVACAINE 1 Intrathecal UNK ML, DAY U 0 QD
127182661 12718266 5 SS DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Intrathecal UNK MG, DAY U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127182661 12718266 1 Pain
127182661 12718266 2 Lumbar radiculopathy

Outcome of event

Event ID CASEID OUTC COD
127182661 12718266 HO
127182661 12718266 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127182661 12718266 Off label use
127182661 12718266 Spinal compression fracture

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

no results found

Therapies reported

no results found