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
124254182 12425418 2 F 20160607 20160601 20160831 PER US-MYLANLABS-2016M1018671 MYLAN 0.00 F Y 0.00000 20160831 CN US US

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
124254182 12425418 1 PS LIDOCAINE PATCH LIDOCAINE 1 1 DF, QD APPLY TO AREA OF PAIN FOR 12 HOURS, REMOVE AND WAIT 12 HOURS TO APPLY NEW PATCH 614311 202346 1 DF CUTANEOUS PATCH QD
124254182 12425418 2 SS LIDOCAINE PATCH LIDOCAINE 1 202346 CUTANEOUS PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124254182 12425418 1 Pain
124254182 12425418 2 Off label use

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124254182 12425418 Drug ineffective for unapproved indication
124254182 12425418 Product quality issue

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

no results found

Therapies reported

no results found