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
127400631 12740063 1 I 20141229 20160908 20160913 20160913 EXP ES-AGEMED-344057440 ES-PFIZER INC-2016424020 PFIZER 71.00 YR M Y 0.00000 20160913 MD ES ES

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
127400631 12740063 1 PS FENTANYL. FENTANYL 1 Transdermal 1 DF, 1X/DAY 2 DF Y 19115 1 DF QD
127400631 12740063 2 I Orfidal LORAZEPAM 1 Oral 1 MG, 1X/DAY Y 74243 1 MG TABLET QD
127400631 12740063 3 I LORMETAZEPAM LORMETAZEPAM 1 Oral 1 DF, 1X/DAY Y 0 1 DF QD
127400631 12740063 4 C LYRICA PREGABALIN 1 Oral 150 MG, 1X/DAY 0 150 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127400631 12740063 1 Medication error

Outcome of event

Event ID CASEID OUTC COD
127400631 12740063 LT
127400631 12740063 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127400631 12740063 Drug interaction
127400631 12740063 Multiple sclerosis
127400631 12740063 Respiratory depression

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
127400631 12740063 1 20141229 20141230 0
127400631 12740063 2 2006 20141230 0
127400631 12740063 3 2007 20141230 0
127400631 12740063 4 201006 20141230 0