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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126938581 | 12693858 | 1 | I | 201608 | 20160819 | 20160829 | 20160829 | PER | US-PFIZER INC-2016397084 | PFIZER | 69.00 | YR | M | Y | 76.00000 | KG | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126938581 | 12693858 | 1 | PS | ALTACE | RAMIPRIL | 1 | 5 MG, UNK | U | 19901 | 5 | MG | ||||||||
| 126938581 | 12693858 | 2 | SS | DILTIAZEM HCL | DILTIAZEM HYDROCHLORIDE | 1 | 120 MG, UNK | U | 74941 | 120 | MG |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126938581 | 12693858 | Agitation | |
| 126938581 | 12693858 | Dizziness | |
| 126938581 | 12693858 | Feeling abnormal | |
| 126938581 | 12693858 | Flushing | |
| 126938581 | 12693858 | Panic reaction | |
| 126938581 | 12693858 | Presyncope |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |