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
127002291 12700229 1 I 20160531 20160822 20160830 20160830 EXP CN-PFIZER INC-2016404549 PFIZER 72.00 YR F Y 56.00000 KG 20160830 OT CN CN

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
127002291 12700229 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, 2X/DAY Y L19071 20699 75 MG PROLONGED-RELEASE CAPSULE BID
127002291 12700229 2 C PAIDISHENG 2 Oral 30 MG, 1X/DAY 15122206 0 30 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127002291 12700229 1 Depression
127002291 12700229 2 Depression

Outcome of event

Event ID CASEID OUTC COD
127002291 12700229 HO
127002291 12700229 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127002291 12700229 Dizziness
127002291 12700229 Heart rate increased
127002291 12700229 Hyperhidrosis
127002291 12700229 Hypertension
127002291 12700229 Nervousness
127002291 12700229 Psychotic disorder

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
127002291 12700229 1 20160401 20160603 0
127002291 12700229 2 20160401 20160606 0