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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7386257 | 7879778 | I | 7386257-6 | 20110312 | 20110323 | 20110331 | EXP | BR-NOVOPROD-325578 | NOVOPROD | 11 | YR | M | Y | 35 | KG | 20110331 | MD | BRAZIL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7386257 | 1016137022 | C | FEIBA | 1 | INTRAVENOUS | ONLY IN CASES OF LESION, PRN EVERY 6 HOURS AND EVERY 12 HOURS | |||||
| 7386257 | 1016137021 | PS | NOVOSEVEN | 1 | INTRAVENOUS | 3 INJECTIONS, WITH 2 AND 3 HOURS BETWEEN EACH INJECTION, ONLY IN CASES OF LESION, PRN | NOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7386257 | 1016137022 | HAEMOPHILIA A WITH ANTI FACTOR VIII |
| 7386257 | 1016137021 | HAEMOPHILIA A WITH ANTI FACTOR VIII |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7386257 | HO |
| 7386257 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7386257 | HAEMORRHAGE |
| 7386257 | THERAPEUTIC RESPONSE DECREASED |
| 7386257 | HYPOVOLAEMIC SHOCK |
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 |
|---|---|---|---|---|---|
| 7386257 | 1016137022 | 20000324 | |||
| 7386257 | 1016137021 | 20090324 |