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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662500 | 7295099 | F | 6662500-3 | 20100214 | 20100329 | 20100331 | EXP | US-MERCK-1002USA03502 | MERCK HUMAN HEALTH DIVISION | 85 | YR | F | Y | 20100401 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662500 | 1013425046 | PS | INVANZ | 1 | INTRAMUSCULAR | 021337 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6662500 | 1013425046 | ESCHERICHIA INFECTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6662500 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6662500 | CONVULSION |
| 6662500 | HALLUCINATION |
| 6662500 | MUSCULAR WEAKNESS |
| 6662500 | MYALGIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6662500 | 1013425046 | 20100211 |