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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127582631 | 12758263 | 1 | I | 20160610 | 20160912 | 20160919 | 20160919 | EXP | GB-MHRA-MIDB-859D8383-E1AF-4CBC-8380-5DD9F6BF039F | GB-GLAXOSMITHKLINE-GB2016132883 | GLAXOSMITHKLINE | 43.00 | YR | M | Y | 0.00000 | 20160919 | PH | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127582631 | 12758263 | 1 | PS | CEFUROXIME. | CEFUROXIME | 1 | Intravenous bolus | UNK, PATIENT CHALLENGED WITH INCREASING DOSES. NO REACTIONS OCCURRED UNTIL FULL DOSE GIVEN AS A BOLU | D | 50605 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127582631 | 12758263 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127582631 | 12758263 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127582631 | 12758263 | Hypotension | |
| 127582631 | 12758263 | Tachycardia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |