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
125667023 12566702 3 F 201511 20160808 20160718 20160810 EXP US-PFIZER INC-2016345759 PFIZER 74.00 YR F Y 54.00000 KG 20160810 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
125667023 12566702 1 PS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 Oral 0.625, 2.5 MG, 1X/DAY L160805 20527 TABLET QD
125667023 12566702 2 SS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 20527 TABLET
125667023 12566702 3 C SYNTHROID LEVOTHYROXINE SODIUM 1 UNK 0
125667023 12566702 4 C ASPIRIN. ASPIRIN 1 81 MG, UNK 0 81 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125667023 12566702 1 Hormone replacement therapy
125667023 12566702 2 Thyroid disorder

Outcome of event

Event ID CASEID OUTC COD
125667023 12566702 HO
125667023 12566702 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125667023 12566702 Circulatory collapse
125667023 12566702 Hypertension
125667023 12566702 Loss of consciousness
125667023 12566702 Malaise
125667023 12566702 Memory impairment
125667023 12566702 Myocardial infarction
125667023 12566702 Pain
125667023 12566702 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found