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
106520583 10652058 3 F 20160725 20141215 20160801 PER US-PFIZER INC-2014343060 PFIZER 53.00 YR F Y 0.00000 20160801 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
106520583 10652058 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 100 MG, 1X/DAY J95648 21992 100 MG PROLONGED-RELEASE TABLET QD
106520583 10652058 2 C CLONAZEPAM. CLONAZEPAM 1 1 MG, 3X/DAY 0 1 MG TID
106520583 10652058 3 C GABAPENTIN. GABAPENTIN 1 UNK 0
106520583 10652058 4 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 UNK 0
106520583 10652058 5 C VITAMIN B12 CYANOCOBALAMIN 1 UNK 0 INJECTION
106520583 10652058 6 C ADVIL IBUPROFEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106520583 10652058 1 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
106520583 10652058 Feeling abnormal
106520583 10652058 Headache
106520583 10652058 Nausea
106520583 10652058 Nightmare
106520583 10652058 Tremor
106520583 10652058 Vertigo
106520583 10652058 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
106520583 10652058 1 2009 0
106520583 10652058 2 2000 0