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
125318721 12531872 1 I 20160510 20160701 20160706 20160706 EXP FR-SA-2016SA123457 AVENTIS 61.00 YR A F Y 0.00000 20160706 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
125318721 12531872 1 SS TIAPRIDAL TIAPRIDE HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNKNOWN 0 1 DF SOLUTION FOR INJECTION 1X
125318721 12531872 2 PS STILNOX ZOLPIDEM TARTRATE 1 Oral Y UNKNOWN 19908 1 DF TABLET
125318721 12531872 3 SS TERCIAN CYAMEMAZINE 1 Oral 30 DROPS OF TERCIAN AT 4:00 AM THEN 50 DROPS AT 12:30. Y UNKNOWN 0 ORAL DROPS, SOLUTION
125318721 12531872 4 SS ZOVIRAX ACYCLOVIR 1 Oral Y UNKNOWN 0
125318721 12531872 5 SS DUROGESIC FENTANYL 1 Cutaneous UNKNOWN 0
125318721 12531872 6 C PHOCYTAN .ALPHA.-GLUCOSE-1-PHOSPHATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125318721 12531872 1 Agitation
125318721 12531872 3 Agitation
125318721 12531872 6 Hypophosphataemia

Outcome of event

Event ID CASEID OUTC COD
125318721 12531872 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125318721 12531872 Coma

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
125318721 12531872 1 20160508 20160508 0
125318721 12531872 2 20160510 0
125318721 12531872 3 20160510 20160510 0
125318721 12531872 4 20160502 20160510 0
125318721 12531872 5 20160508 20160508 0
125318721 12531872 6 20160509 0