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
126796252 12679625 2 F 20160723 20160822 20160824 20160830 PER US-PFIZER INC-2016367487 PFIZER 3.00 YR F Y 0.00000 20160830 OT 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
126796252 12679625 1 PS Genotropin MQ SOMATROPIN 1 Subcutaneous 0.6 MG, DAILY (AT BED TIME) U 20280 .6 MG POWDER FOR SOLUTION FOR INJECTION
126796252 12679625 2 SS Genotropin MQ SOMATROPIN 1 U 20280 POWDER FOR SOLUTION FOR INJECTION
126796252 12679625 3 C CORTEF HYDROCORTISONE 1 0
126796252 12679625 4 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 0
126796252 12679625 5 C SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126796252 12679625 1 Growth hormone deficiency
126796252 12679625 2 Hypopituitarism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126796252 12679625 Injection site pain
126796252 12679625 Vomiting

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
126796252 12679625 1 20150826 0