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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5282290 | 6274020 | F | 5282290-9 | 20060920 | 20070320 | 20070331 | EXP | FR-PFIZER INC-2007023761 | PFIZER INC | F | Y | 69 | KG | 20070330 | MD | FRANCE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5282290 | 1008316852 | PS | LYRICA | 1 | ORAL | 021446 | |||||
5282290 | 1008316853 | C | ALL OTHER THERAPEUTIC PRODUCTS | 2 | |||||||
5282290 | 1008316854 | C | LEVOTHYROXINE SODIUM | 1 | ORAL | ||||||
5282290 | 1008316855 | C | CYAMEMAZINE | 2 | ORAL | ||||||
5282290 | 1008316856 | C | ACEPROMETAZINE | 2 | ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5282290 | 1008316852 | POST HERPETIC NEURALGIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5282290 | OT |
Reactions reported
Event ID | PT |
---|---|
5282290 | BLOOD PRESSURE INCREASED |
5282290 | DYSPNOEA |
5282290 | HYPERSENSITIVITY |
5282290 | NAUSEA |
5282290 | RESPIRATORY DEPRESSION |
5282290 | TACHYCARDIA |
5282290 | VERTIGO |
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 |
---|---|---|---|---|---|
5282290 | 1008316852 | 20060919 | 20060929 |