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
108750208 10875020 8 F 201412 20160801 20150227 20160816 EXP US-JAZZ-2014-US-016932 JAZZ 69.04 YR F Y 0.00000 20160816 CN 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
108750208 10875020 1 PS PRIALT ZICONOTIDE ACETATE 1 Intrathecal UNK ?G, QH Y 18860-0720-10 21060
108750208 10875020 2 SS PRIALT ZICONOTIDE ACETATE 1 Intrathecal 0.104 ?G, QH Y 21060 .104 UG
108750208 10875020 3 SS PRIALT ZICONOTIDE ACETATE 1 Intrathecal 0.104 ?G, QH Y 21060 .104 UG
108750208 10875020 4 SS PRIALT ZICONOTIDE ACETATE 1 Intrathecal UNK ?G, QH Y 21060
108750208 10875020 5 SS MORPHINE SULFATE. MORPHINE SULFATE 1 Intrathecal 0.145 MG, QH U 0 .145 MG INJECTION
108750208 10875020 6 SS MORPHINE SULFATE. MORPHINE SULFATE 1 U 0 INJECTION
108750208 10875020 7 SS MORPHINE SULFATE. MORPHINE SULFATE 1 U 0 INJECTION
108750208 10875020 8 C MORPHINE SULFATE. MORPHINE SULFATE 1 Oral U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108750208 10875020 1 Spinal pain
108750208 10875020 2 Pain
108750208 10875020 3 Neuropathy peripheral
108750208 10875020 5 Spinal pain
108750208 10875020 6 Pain
108750208 10875020 7 Neuropathy peripheral

Outcome of event

Event ID CASEID OUTC COD
108750208 10875020 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108750208 10875020 Abdominal distension
108750208 10875020 Constipation
108750208 10875020 Drug ineffective
108750208 10875020 Herpes simplex
108750208 10875020 Memory impairment
108750208 10875020 Oedema
108750208 10875020 Pain
108750208 10875020 Peripheral swelling
108750208 10875020 Scar
108750208 10875020 Scoliosis
108750208 10875020 Skin discolouration
108750208 10875020 Swelling

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
108750208 10875020 1 20141210 0
108750208 10875020 2 20150213 0
108750208 10875020 3 20150213 0
108750208 10875020 4 201505 0