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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127803371 | 12780337 | 1 | I | 20160726 | 20160919 | 20160926 | 20160926 | EXP | FR-PFIZER INC-2016439125 | PFIZER | 47.00 | YR | F | Y | 0.00000 | 20160926 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127803371 | 12780337 | 1 | PS | PAMIDRONATE DISODIUM. | PAMIDRONATE DISODIUM | 1 | Intravenous drip | 90 MG, SINGLE | Y | 75841 | 90 | MG | |||||||
| 127803371 | 12780337 | 2 | SS | PAMIDRONATE DISODIUM. | PAMIDRONATE DISODIUM | 1 | Intravenous drip | 45 MG, SINGLE | Y | 75841 | 45 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127803371 | 12780337 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127803371 | 12780337 | Cough | |
| 127803371 | 12780337 | Headache | |
| 127803371 | 12780337 | Malaise | |
| 127803371 | 12780337 | Nausea | |
| 127803371 | 12780337 | Presyncope | |
| 127803371 | 12780337 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127803371 | 12780337 | 1 | 20160726 | 20160726 | 0 | |
| 127803371 | 12780337 | 2 | 20160728 | 20160728 | 0 |