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
125975371 12597537 1 I 20160629 20160727 20160727 PER US-PFIZER INC-2016325079 PFIZER 0.00 Y 0.00000 20160727 MD 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
125975371 12597537 1 PS DICLOFENAC EPOLAMINE DICLOFENAC EPOLAMINE 1 UNK U 21234
125975371 12597537 2 SS FENTANYL CITRATE. FENTANYL CITRATE 1 UNK U 72786 SOLUTION FOR INJECTION
125975371 12597537 3 SS LIDOCAINE HCL LIDOCAINE HYDROCHLORIDE 1 UNK U 17549
125975371 12597537 4 SS METOCLOPRAMIDE HCL METOCLOPRAMIDE HYDROCHLORIDE 1 UNK U 73118
125975371 12597537 5 SS PHENTOLAMINE PHENTOLAMINE 1 UNK U 0
125975371 12597537 6 SS SULFABENZAMIDE. SULFABENZAMIDE 1 UNK U 0
125975371 12597537 7 SS SULFATHIAZOLE SULFATHIAZOLE 1 UNK U 0
125975371 12597537 8 SS SODIUM SODIUM 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125975371 12597537 Drug hypersensitivity

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

no results found

Therapies reported

no results found