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
126772012 12677201 2 F 20160913 20160823 20160919 PER US-PFIZER INC-2016375700 PFIZER 62.00 YR F Y 65.00000 KG 20160919 CN 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
126772012 12677201 1 PS PREMARIN ESTROGENS, CONJUGATED 1 Oral 0.3 MG, 1X/DAY N 4782 .3 MG TABLET QD
126772012 12677201 2 SS PREMARIN ESTROGENS, CONJUGATED 1 0.3 UNK, UNK (3 WEEKS) N 4782 .3 MG TABLET QD
126772012 12677201 3 C SIMVASTATIN. SIMVASTATIN 1 Oral 20 MG, 1X/DAY 0 20 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126772012 12677201 1 Menopause
126772012 12677201 3 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126772012 12677201 Drug ineffective
126772012 12677201 Irritability
126772012 12677201 Malaise
126772012 12677201 Mood altered

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
126772012 12677201 1 2016 20160802 0