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
125088622 12508862 2 F 20160615 20160701 20160629 20160712 EXP IT-PFIZER INC-2016310938 PFIZER 74.00 YR F Y 0.00000 20160712 PH IT IT

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
125088622 12508862 1 PS HALCION TRIAZOLAM 1 Oral 0.125 MG, DAILY Y A152297B 17892 .125 MG TABLET
125088622 12508862 2 C TORVAST ATORVASTATIN 1 Oral 10 MG, DAILY 0 10 MG TABLET
125088622 12508862 3 C NERIXIA NERIDRONIC ACID 1 ONE VIAL, WEEKLY 0 1 DF /wk
125088622 12508862 4 C CAFERGOT CAFFEINEERGOTAMINE TARTRATE 1 A TABLET, IN THE EVENING 0 1 DF TABLET
125088622 12508862 5 C RILAMIG 2 1 DF, AS NEEDED 0 1 DF TABLET
125088622 12508862 6 C RIFACOL RIFAXIMIN 1 MONTHLY CYCLES 0 /month
125088622 12508862 7 C BROMAZEPAM BROMAZEPAM 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125088622 12508862 1 Insomnia
125088622 12508862 5 Migraine

Outcome of event

Event ID CASEID OUTC COD
125088622 12508862 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125088622 12508862 Glossodynia
125088622 12508862 Rectal haemorrhage

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found