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
126591331 12659133 1 I 2016 20160805 20160817 20160817 EXP CA-PFIZER INC-2016379133 PFIZER 0.00 F Y 0.00000 20160817 CN CA CA

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
126591331 12659133 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY Y 21992 50 MG PROLONGED-RELEASE TABLET QD
126591331 12659133 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Y 21992 PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126591331 12659133 1 Depression
126591331 12659133 2 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126591331 12659133 OT
126591331 12659133 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126591331 12659133 Cough
126591331 12659133 Dysphonia
126591331 12659133 Dyspnoea
126591331 12659133 Intentional product misuse
126591331 12659133 Migraine
126591331 12659133 Nasopharyngitis
126591331 12659133 Nausea
126591331 12659133 Respiratory arrest
126591331 12659133 Sensation of foreign body
126591331 12659133 Withdrawal syndrome

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
126591331 12659133 1 201606 201607 0