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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125866231 | 12586623 | 1 | I | 20160629 | 20160725 | 20160725 | PER | US-PFIZER INC-2016326247 | PFIZER | 38.00 | YR | F | Y | 138.00000 | KG | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125866231 | 12586623 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | UNK | U | 18989 | ||||||||||
125866231 | 12586623 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | U | 18989 | |||||||||||
125866231 | 12586623 | 3 | SS | TYLENOL | ACETAMINOPHEN | 1 | UNK | U | 0 | ||||||||||
125866231 | 12586623 | 4 | SS | TYLENOL | ACETAMINOPHEN | 1 | U | 0 | |||||||||||
125866231 | 12586623 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | 1000 MG, 2X/DAY | 0 | 1000 | MG | BID | ||||||||
125866231 | 12586623 | 6 | C | GABAPENTIN. | GABAPENTIN | 1 | 300 MG, 2X/DAY | 0 | 300 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125866231 | 12586623 | 1 | Feeling abnormal |
125866231 | 12586623 | 2 | Pain |
125866231 | 12586623 | 3 | Feeling abnormal |
125866231 | 12586623 | 4 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125866231 | 12586623 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |