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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022290 | 7612839 | I | 7022290-1 | 20100912 | 20100922 | 20100930 | EXP | JP-JNJFOC-20100907809 | JOHNSON + JOHNSON HEALTHCARE PRODUCTS | 60 | YR | M | Y | 20100930 | MD | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022290 | 1014808946 | PS | MICONAZOLE NITRATE | 1 | OROPHARINGEAL | UNSPECIFIED | 17450 | ||||
| 7022290 | 1014808947 | SS | MICONAZOLE NITRATE | 1 | OROPHARINGEAL | 10G OF GEL (2.5G OF GEL 4 TIMES) PER DAY | UNSPECIFIED | 017450 | |||
| 7022290 | 1014808948 | I | WARFARIN SODIUM | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7022290 | 1014808947 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7022290 | 1014808948 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7022290 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7022290 | DRUG INTERACTION |
| 7022290 | PERICARDIAL HAEMORRHAGE |
| 7022290 | PULMONARY HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |