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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5742762 | 6643490 | I | 5742762-7 | 20071126 | 20080509 | 20080519 | EXP | CG-MERCK-0805USA02190 | MERCK HUMAN HEALTH DIVISION | 28 | YR | M | Y | 20080519 | MD | CONGO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5742762 | 1009925563 | PS | STROMECTOL | 1 | ORAL | 050742 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5742762 | 1009925563 | ONCHOCERCIASIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5742762 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5742762 | HEADACHE |
| 5742762 | MYALGIA |
| 5742762 | OCULAR HYPERAEMIA |
| 5742762 | PARESIS |
| 5742762 | PYREXIA |
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 |
|---|---|---|---|---|---|
| 5742762 | 1009925563 | 20071125 | 20071125 | 1 | DAY |