Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6540467 | 7553394 | I | 6540467-6 | 20100105 | 20100113 | EXP | 467054 | HOSPIRA, INC. | 86 | YR | M | N | 59 | KG | 20100112 | OT | CANADA |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6540467 | 1012954985 | PS | ACYCLOVIR SODIUM | 1 | INTRAVENOUS | 1000 MG DOSE EVERY 12 HOURS, INTRAVENOUS | D | D | 74720 | ||
| 6540467 | 1012998925 | C | ACETAMINOPHEN | 1 | 74720 | ||||||
| 6540467 | 1012998927 | C | AVODART | 1 | 74720 | ||||||
| 6540467 | 1012998928 | C | CEFTRIAXONE | 1 | 74720 | ||||||
| 6540467 | 1012998930 | C | DIMENHYDRINATE | 1 | 74720 | ||||||
| 6540467 | 1012998931 | C | DOCUSATE | 2 | 74720 | ||||||
| 6540467 | 1012998932 | C | HEPARIN SODIUM | 1 | 74720 | ||||||
| 6540467 | 1012998933 | C | ALBUTEROL SULFATE AUTOHALER | 1 | 74720 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6540467 | 1012954985 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6540467 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 6540467 | BLOOD CREATININE INCREASED |
| 6540467 | DEPRESSED LEVEL OF CONSCIOUSNESS |
| 6540467 | DYSKINESIA |
| 6540467 | LOSS OF CONSCIOUSNESS |
| 6540467 | MUSCLE SPASTICITY |
| 6540467 | MYOCLONUS |
| 6540467 | NUCHAL RIGIDITY |
| 6540467 | OPISTHOTONUS |
| 6540467 | OROPHARYNGEAL SPASM |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6540467 | FGN |
| 6540467 | HP |
| 6540467 | OTH |
Therapies reported
| no results found |