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
127403991 12740399 1 I 201608 20160905 20160913 20160913 EXP SE-MUNDIPHARMA DS AND PHARMACOVIGILANCE-GBR-2016-0040484 PURDUE 83.00 YR F Y 0.00000 20160913 MD SE SE

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
127403991 12740399 1 PS DOLCONTIN MORPHINE 1 Unknown 20 MG, BID U 19516 20 MG PROLONGED-RELEASE TABLET
127403991 12740399 2 SS AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 Unknown 5 MG, BID 0 5 MG
127403991 12740399 3 SS NAPROXEN. NAPROXEN 1 Unknown 500 MG, BID 0 500 MG
127403991 12740399 4 C ALVEDON ACETAMINOPHEN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127403991 12740399 1 Back pain
127403991 12740399 2 Hypertension
127403991 12740399 3 Back pain
127403991 12740399 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127403991 12740399 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127403991 12740399 Acute kidney injury
127403991 12740399 Hypotension
127403991 12740399 Sedation

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
127403991 12740399 1 201608 0
127403991 12740399 2 201608 201608 0
127403991 12740399 3 201608 0
127403991 12740399 4 201608 0