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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7299194 | 7377474 | F | 7299194-2 | 20100101 | 20110209 | 20110217 | EXP | US-PFIZER INC-2010054283 | PFIZERINC | YR | F | Y | 20110216 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7299194 | 1015807219 | C | LAMICTAL | 1 | UNK | ||||||
7299194 | 1015807221 | C | ADDERALL 10 | 1 | UNK | ||||||
7299194 | 1015807217 | PS | ZOLOFT | 1 | 200 MG, DAILY | 019839 | |||||
7299194 | 1015807220 | C | ABILIFY | 1 | UNK | ||||||
7299194 | 1015807218 | SS | PRISTIQ | 1 | 50 MG, DAILY | 189412005469 | 021992 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7299194 | 1015807217 | DEPRESSION |
7299194 | 1015807218 | DEPRESSION |
Outcome of event
Event ID | OUTC COD |
---|---|
7299194 | OT |
Reactions reported
Event ID | PT |
---|---|
7299194 | STAPHYLOCOCCAL INFECTION |
7299194 | DRUG INEFFECTIVE |
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 |
---|---|---|---|---|---|
7299194 | 1015807217 | 20100101 | |||
7299194 | 1015807218 | 20100401 |