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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6537380 | 7487157 | F | 6537380-7 | 20081101 | 20100106 | 20100114 | EXP | US-NOVOPROD-291190 | NOVOPROD | 70 | YR | F | Y | 20100114 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6537380 | 1012942100 | PS | ACTIVELLA | 1 | ORAL | UNKNOWN | VF70136 | 20907 | |||
| 6537380 | 1012942101 | SS | ACTIVELLA | 1 | 020907 | ||||||
| 6537380 | 1012942102 | C | LEXAPRO | 1 | ORAL | ||||||
| 6537380 | 1012942103 | C | XANAX | 1 | ORAL | ||||||
| 6537380 | 1012942104 | C | DIOVAN /01319601/ | 2 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6537380 | 1012942100 | VULVOVAGINAL DRYNESS |
| 6537380 | 1012942101 | VULVOVAGINAL BURNING SENSATION |
| 6537380 | 1012942102 | ANXIETY |
| 6537380 | 1012942103 | SLEEP DISORDER |
| 6537380 | 1012942104 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6537380 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6537380 | CEREBROVASCULAR ACCIDENT |
| 6537380 | VISION BLURRED |
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 |
|---|---|---|---|---|---|
| 6537380 | 1012942100 | 20070101 | |||
| 6537380 | 1012942102 | 20080101 | |||
| 6537380 | 1012942103 | 19990101 |