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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125318201 | 12531820 | 1 | I | 20160630 | 20160706 | 20160706 | PER | US-PFIZER INC-2016327550 | PFIZER | 0.00 | M | Y | 0.00000 | 20160706 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125318201 | 12531820 | 1 | SS | CODEINE PHOSPHATE | CODEINE PHOSPHATE | 1 | UNK | U | 0 | ||||||||||
125318201 | 12531820 | 2 | PS | DEXTROSE. | DEXTROSE | 1 | UNK | U | 16367 | ||||||||||
125318201 | 12531820 | 3 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | UNK | U | 19999 | ||||||||||
125318201 | 12531820 | 4 | SS | SODIUM CHLORIDE. | SODIUM CHLORIDE | 1 | UNK | U | 19480 | SOLUTION FOR INJECTION | |||||||||
125318201 | 12531820 | 5 | SS | PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN | ACETAMINOPHENPROPOXYPHENE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
125318201 | 12531820 | 6 | SS | TRAMADOL HCL | TRAMADOL HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
125318201 | 12531820 | 7 | SS | HYDROCODONE | HYDROCODONE | 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 |
---|---|---|---|
125318201 | 12531820 | Confusional state | |
125318201 | 12531820 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |