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
126736191 12673619 1 I 20160817 20160822 20160822 PER US-PFIZER INC-2016393284 PFIZER 0.00 F Y 0.00000 20160822 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
126736191 12673619 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 150 MG, 1X/DAY N39354 21992 150 MG PROLONGED-RELEASE TABLET QD
126736191 12673619 2 C BIESTROGEN 2 1 DF, 1X/DAY (BIEST 0.25 MG, ONE CAPSULE A DAY) 0 1 DF QD
126736191 12673619 3 C PROGESTERONE. PROGESTERONE 1 100 MG, UNK 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126736191 12673619 2 Hormone replacement therapy
126736191 12673619 3 Hormone replacement therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126736191 12673619 Dizziness
126736191 12673619 Eye pain
126736191 12673619 Eye swelling
126736191 12673619 Metamorphopsia
126736191 12673619 Ocular discomfort
126736191 12673619 Vertigo
126736191 12673619 Visual impairment

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

no results found

Therapies reported

no results found