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 |