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
126199251 12619925 1 I 201508 20160719 20160803 20160803 EXP US-SAOL THERAPEUTICS-2016SAO00311 SAOL THERAPEUTICS 0.00 F Y 0.00000 20160803 CN COUNTRY NOT SPECIFIED 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
126199251 12619925 1 PS COMPOUNDED BACLOFEN BACLOFEN 1 Intrathecal U U 20075 INJECTION
126199251 12619925 2 SS COMPOUNDED BACLOFEN BACLOFEN 1 U U 20075 INJECTION
126199251 12619925 3 SS HYDROMORPHONE HYDROMORPHONE 1 Intrathecal U 0
126199251 12619925 4 SS CLONIDINE. CLONIDINE 1 Intrathecal U 0
126199251 12619925 5 SS DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Intrathecal U 0
126199251 12619925 6 SS OTHER UNSPECIFIED INGREDIENT 1 Intrathecal U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126199251 12619925 1 Pain
126199251 12619925 2 Post herpetic neuralgia

Outcome of event

Event ID CASEID OUTC COD
126199251 12619925 HO
126199251 12619925 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126199251 12619925 Device alarm issue
126199251 12619925 Hospitalisation
126199251 12619925 Kidney infection
126199251 12619925 Off label use
126199251 12619925 Sepsis
126199251 12619925 Therapy cessation

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

no results found

Therapies reported

no results found