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
124853452 12485345 2 F 20140903 20160713 20160621 20160715 EXP NL-PFIZER INC-2015281473 PFIZER 82.00 YR F Y 0.00000 20160715 MD NL NL

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
124853452 12485345 1 PS SOMAVERT PEGVISOMANT 1 Subcutaneous UNK 21106 POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
124853452 12485345 2 SS SOMAVERT PEGVISOMANT 1 Subcutaneous 30 MG, WEEKLY 21106 30 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION /wk
124853452 12485345 3 SS SOMAVERT PEGVISOMANT 1 Subcutaneous 30 MG, 1X/DAY 21106 30 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124853452 12485345 1 Acromegaly

Outcome of event

Event ID CASEID OUTC COD
124853452 12485345 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124853452 12485345 Off label use
124853452 12485345 Organ failure
124853452 12485345 Sense of oppression

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
124853452 12485345 1 20040809 0
124853452 12485345 2 20140903 20141201 0
124853452 12485345 3 20141202 201606 0