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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126134591 | 12613459 | 1 | I | 20160705 | 0 | 20160801 | 20160801 | DIR | 84.00 | YR | M | N | 197.00000 | LBS | 20160720 | N | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126134591 | 12613459 | 1 | PS | ROCEPHIN | CEFTRIAXONE SODIUM | 1 | Intramuscular | 1GM ONE TIME IM DOSE IM RIGHT VENTROGLUETAL | Y | N | 590448M | 20181101 | 0 | 1 | G | 1X |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126134591 | 12613459 | 1 | Cough |
| 126134591 | 12613459 | 1 | Nasal congestion |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126134591 | 12613459 | Dizziness | |
| 126134591 | 12613459 | Dyspnoea | |
| 126134591 | 12613459 | Electrocardiogram abnormal | |
| 126134591 | 12613459 | Eye movement disorder | |
| 126134591 | 12613459 | Loss of consciousness | |
| 126134591 | 12613459 | Paraesthesia oral | |
| 126134591 | 12613459 | Pulse absent |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 126134591 | 12613459 | HP |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126134591 | 12613459 | 1 | 20160705 | 0 |