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
126248891 12624889 1 I 2016 20160801 20160805 20160805 PER US-PFIZER INC-2016371694 PFIZER 64.00 YR F Y 82.00000 KG 20160805 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
126248891 12624889 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 100 MG, 1X/DAY 21992 100 MG PROLONGED-RELEASE TABLET QD
126248891 12624889 2 SS REXULTI BREXPIPRAZOLE 1 2 MG, 1X/DAY BMS00116 0 2 MG TABLET QD
126248891 12624889 3 C CLONAZEPAM. CLONAZEPAM 1 1 MG, UNK 0 1 MG
126248891 12624889 4 C CLONAZEPAM. CLONAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126248891 12624889 1 Depression
126248891 12624889 2 Depression
126248891 12624889 3 Nervousness
126248891 12624889 4 Sleep disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126248891 12624889 Condition aggravated
126248891 12624889 Depression
126248891 12624889 Dizziness
126248891 12624889 Increased appetite

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
126248891 12624889 2 20160509 20160609 0