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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6775383 | 7423786 | I | 6775383-8 | 20100310 | 20100609 | 20100617 | EXP | FR-PFIZER INC-2010071984 | PFIZERINC | 90 | YR | F | Y | 20100617 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6775383 | 1013888300 | PS | ALDACTONE | 1 | ORAL | 75 MG, 1X/DAY | 12151 | ||||
| 6775383 | 1013888301 | SS | ACTOS | 1 | ORAL | 30 MG, 1X/DAY | |||||
| 6775383 | 1013888302 | SS | CARDENSIEL | 2 | ORAL | 2.5 MG, UNK | |||||
| 6775383 | 1013888303 | SS | LEVOTHYROXINE SODIUM | 1 | ORAL | 100 UG, 1X/DAY | |||||
| 6775383 | 1013888304 | SS | COVERSYL | 2 | ORAL | UNK MG, UNK | |||||
| 6775383 | 1013888305 | SS | AMAREL | 2 | ORAL | 2 MG, UNK | |||||
| 6775383 | 1013888306 | SS | LASIX | 1 | ORAL | 40 MG, 2X/WEEK | |||||
| 6775383 | 1013888307 | SS | DIFFU K | 2 | ORAL | 1 DF, 1X/DAY | |||||
| 6775383 | 1013888308 | SS | PREVISCAN | 2 | ORAL | 15 MG, 1X/DAY |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6775383 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6775383 | CARDIAC FAILURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |