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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6919447 | 7537111 | I | 6919447-4 | 20100709 | 20100803 | 20100811 | EXP | B0668231A | GLAXOSMITHKLINE | 47 | YR | F | Y | 20100811 | CN | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6919447 | 1014394008 | PS | WELLVONE | 2 | ORAL | 750MG TWICE PER DAY | UNKNOWN | 20500 | |||
| 6919447 | 1014394009 | SS | CLINDAMYCIN HCL | 1 | INTRAVENOUS | 600MG FOUR TIMES PER DAY | UNKNOWN | ||||
| 6919447 | 1014394010 | SS | MALOCIDE | 2 | ORAL | UNKNOWN | 008578 | ||||
| 6919447 | 1014394011 | SS | KEPPRA | 1 | ORAL | UNKNOWN | |||||
| 6919447 | 1014394012 | SS | TOPALGIC (FRANCE) | 2 | ORAL | 50MG TWICE PER DAY | UNKNOWN | ||||
| 6919447 | 1014394013 | SS | PRIMPERAN TAB | 1 | ORAL | 1UNIT THREE TIMES PER DAY | UNKNOWN | ||||
| 6919447 | 1014394014 | SS | ATRIPLA | 1 | ORAL | 1UNIT PER DAY | UNKNOWN | ||||
| 6919447 | 1014394015 | SS | IDARAC | 1 | ORAL | UNKNOWN | |||||
| 6919447 | 1014394016 | SS | SPECIAFOLDINE | 2 | UNKNOWN | UNKNOWN | |||||
| 6919447 | 1014394017 | C | ATARAX | 1 | ORAL | 25MG PER DAY | UNKNOWN | ||||
| 6919447 | 1014394018 | C | LEXOMIL | 2 | UNKNOWN | .5UNIT PER DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6919447 | 1014394009 | CEREBRAL TOXOPLASMOSIS |
| 6919447 | 1014394010 | CEREBRAL TOXOPLASMOSIS |
| 6919447 | 1014394011 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394012 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394013 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394014 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394015 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394016 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394017 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6919447 | 1014394018 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6919447 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6919447 | NEUTROPENIA |
| 6919447 | THROMBOCYTOPENIA |
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 |
|---|---|---|---|---|---|
| 6919447 | 1014394008 | 20100625 | 20100702 | 8 | DAY |
| 6919447 | 1014394009 | 20100630 | 20100709 | 10 | DAY |
| 6919447 | 1014394010 | 20100629 | 20100712 | 14 | DAY |
| 6919447 | 1014394011 | 20100629 | 20100712 | 14 | DAY |
| 6919447 | 1014394012 | 20100624 | 20100702 | 9 | DAY |
| 6919447 | 1014394013 | 20100702 | 20100705 | 4 | DAY |
| 6919447 | 1014394014 | 20090701 | 20100709 | ||
| 6919447 | 1014394015 | 20100628 | 20100710 | 13 | DAY |
| 6919447 | 1014394016 | 20100711 | |||
| 6919447 | 1014394017 | 20100705 |