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
125948701 12594870 1 I 20160623 20160721 20160726 20160726 EXP FR-PFIZER INC-2016355723 PFIZER 26.00 YR M Y 0.00000 20160726 OT FR FR

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
125948701 12594870 1 PS XANAX ALPRAZOLAM 1 Oral UNK 18276 TABLET
125948701 12594870 2 SS ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Oral UNK 0
125948701 12594870 3 SS VALIUM DIAZEPAM 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125948701 12594870 1 Social anxiety disorder
125948701 12594870 2 Social anxiety disorder
125948701 12594870 3 Social anxiety disorder

Outcome of event

Event ID CASEID OUTC COD
125948701 12594870 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125948701 12594870 Dizziness
125948701 12594870 Dyspnoea
125948701 12594870 Hyperhidrosis
125948701 12594870 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
125948701 12594870 1 2015 20160623 0
125948701 12594870 2 2015 20160623 0
125948701 12594870 3 2015 20160623 0