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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7117089 | 7571074 | F | 7117089-1 | 20061101 | 20101118 | 20101122 | PER | US-PFIZER INC-2010107149 | PFIZERINC | 49 | YR | F | Y | 20101122 | LW | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7117089 | 1015166111 | PS | CHANTIX | 1 | UNK | 021928 | |||||
7117089 | 1015166112 | C | ZOLOFT | 1 | UNK | ||||||
7117089 | 1015166113 | C | OXYCODONE | 2 | UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7117089 | 1015166111 | SMOKING CESSATION THERAPY |
7117089 | 1015166112 | DEPRESSION |
7117089 | 1015166113 | PAIN |
Outcome of event
Event ID | OUTC COD |
---|---|
7117089 | OT |
Reactions reported
Event ID | PT |
---|---|
7117089 | ABNORMAL DREAMS |
7117089 | AGGRESSION |
7117089 | ANXIETY |
7117089 | DEPRESSION |
7117089 | SUICIDAL IDEATION |
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 |
---|---|---|---|---|---|
7117089 | 1015166111 | 20061101 | 20091001 | ||
7117089 | 1015166112 | 19970101 | |||
7117089 | 1015166113 | 19970101 |