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
117475295 11747529 5 F 20150518 20160727 20151117 20160802 EXP JP-PFIZER INC-2015389940 PFIZER 64.00 YR F Y 56.00000 KG 20160802 MD JP JP

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
117475295 11747529 1 PS SOMAVERT PEGVISOMANT 1 Subcutaneous 40 MG, 1X/DAY 610 MG 21106 40 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QD
117475295 11747529 2 SS SOMAVERT PEGVISOMANT 1 Subcutaneous 10 MG, 1X/DAY 610 MG 21106 10 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QD
117475295 11747529 3 SS SOMAVERT PEGVISOMANT 1 Subcutaneous 30 MG, DAILY 610 MG 21106 30 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117475295 11747529 1 Acromegaly

Outcome of event

Event ID CASEID OUTC COD
117475295 11747529 HO
117475295 11747529 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
117475295 11747529 Disease progression
117475295 11747529 Pituitary tumour

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
117475295 11747529 1 20150318 20150318 0
117475295 11747529 2 20150320 20150515 0
117475295 11747529 3 20160314 0