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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016619 | 8317510 | I | 8016619-5 | 20080101 | 20111220 | 20111231 | EXP | CHPA2011US018400 | NOVARTIS CONSUMER HEALTH, INC. | 51 | YR | F | Y | 20111231 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016619 | 1018419890 | PS | NICOTINE | 1 | TRANSDERMAL | 21 MG, ONCE/SINGLE | 020076 | ||||
| 8016619 | 1018419893 | SS | NICOTINE | 1 | TRANSDERMAL | 21 MG, QD | 020076 | ||||
| 8016619 | 1018419891 | SS | NICOTINE | 1 | TRANSDERMAL | 7 MG, QD | 020076 | ||||
| 8016619 | 1018419892 | SS | NICOTINE | 1 | TRANSDERMAL | 14 MG, QD | 020076 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016619 | 1018419890 | SMOKING CESSATION THERAPY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016619 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8016619 | EXPIRED DRUG ADMINISTERED |
| 8016619 | CHRONIC OBSTRUCTIVE PULMONARY DISEASE |
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 |
|---|---|---|---|---|---|
| 8016619 | 1018419890 | 20111219 | 20111220 | 2 | DAY |
| 8016619 | 1018419893 | 20030101 | 20030101 | ||
| 8016619 | 1018419891 | 20030101 | 20030101 | ||
| 8016619 | 1018419892 | 20030101 | 20030101 |