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
124922522 12492252 2 F 20150107 20160913 20160623 20160915 EXP US-PFIZER INC-2016313318 PFIZER 63.00 YR M Y 0.00000 20160915 LW 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
124922522 12492252 1 PS DEPO-TESTOSTERONE TESTOSTERONE CYPIONATE 1 UNK U 85635 SOLUTION FOR INJECTION
124922522 12492252 2 SS TESTOSTERONE CYPIONATE. TESTOSTERONE CYPIONATE 1 UNK, EVERY 3 WEEKS U 0 Q3W
124922522 12492252 3 C METOPROLOL. METOPROLOL 1 UNK 0
124922522 12492252 4 C LASIX FUROSEMIDE 1 UNK 0
124922522 12492252 5 C POTASSIUM POTASSIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124922522 12492252 1 Hormone replacement therapy
124922522 12492252 2 Hormone replacement therapy
124922522 12492252 3 Hypertension
124922522 12492252 4 Fluid retention
124922522 12492252 5 Blood potassium decreased

Outcome of event

Event ID CASEID OUTC COD
124922522 12492252 DE
124922522 12492252 HO
124922522 12492252 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124922522 12492252 Cardiac failure congestive
124922522 12492252 Myocardial infarction

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
124922522 12492252 1 201412 2015 0
124922522 12492252 2 2011 2013 0
124922522 12492252 3 2007 2015 0
124922522 12492252 4 2013 2015 0
124922522 12492252 5 2013 2015 0