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
124433984 12443398 4 F 20160524 20160829 20160607 20160901 EXP US-PFIZER INC-2016288408 PFIZER 82.00 YR F Y 73.00000 KG 20160901 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
124433984 12443398 1 PS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.625 MG, 1X/DAY L27206 4782 .625 MG TABLET QD
124433984 12443398 2 SS PREMARIN ESTROGENS, CONJUGATED 1 UNK N04346 4782 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124433984 12443398 1 Hormone replacement therapy

Outcome of event

Event ID CASEID OUTC COD
124433984 12443398 OT
124433984 12443398 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124433984 12443398 Asthenia
124433984 12443398 Blood pressure abnormal
124433984 12443398 Crying
124433984 12443398 Depression
124433984 12443398 Drug dose omission
124433984 12443398 Headache
124433984 12443398 Heart rate increased
124433984 12443398 Hypertension
124433984 12443398 Lipids abnormal
124433984 12443398 Malaise
124433984 12443398 Nervousness

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
124433984 12443398 1 1977 0