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
127579681 12757968 1 I 2014 20160914 20160919 20160919 PER US-PFIZER INC-2016433796 PFIZER 0.00 M Y 0.00000 20160919 MD 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
127579681 12757968 1 PS SOMAVERT PEGVISOMANT 1 Subcutaneous 10MG, DAILY Y 21106 10 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
127579681 12757968 2 SS SOMAVERT PEGVISOMANT 1 Subcutaneous 20 MG, DAILY Y 21106 20 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
127579681 12757968 3 C OCTREOTIDE. OCTREOTIDE 1 Intramuscular 40MG, EVERY MONTH 0 40 MG /month
127579681 12757968 4 C CABERGOLINE. CABERGOLINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127579681 12757968 1 Acromegaly
127579681 12757968 3 Acromegaly
127579681 12757968 4 Acromegaly

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127579681 12757968 Arthralgia
127579681 12757968 Drug ineffective
127579681 12757968 Intentional product use issue
127579681 12757968 Musculoskeletal stiffness

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
127579681 12757968 1 2014 0
127579681 12757968 2 201411 0