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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7205775 | 7745358 | I | 7205775-4 | 20101220 | 20101229 | 20101231 | EXP | US-PFIZER INC-2010181381 | PFIZERINC | 71 | YR | M | Y | 86 | KG | 20101230 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7205775 | 1015450449 | PS | LIPITOR | 1 | ORAL | 20 MG, 1X/DAY | 020702 | ||||
7205775 | 1015450450 | SS | LIPITOR | 1 | 10 MG, 1X/DAY | 020702 | |||||
7205775 | 1015450451 | C | IMURAN | 1 | ORAL | 100 MG, 1X/DAY | |||||
7205775 | 1015450452 | C | MESTINON | 1 | ORAL | 60 MG, 4X/DAY |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7205775 | 1015450449 | CARDIAC OPERATION |
7205775 | 1015450451 | MYASTHENIA GRAVIS |
7205775 | 1015450452 | MYASTHENIA GRAVIS |
Outcome of event
Event ID | OUTC COD |
---|---|
7205775 | OT |
Reactions reported
Event ID | PT |
---|---|
7205775 | HEPATITIS A |
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 |
---|---|---|---|---|---|
7205775 | 1015450449 | 20080501 | |||
7205775 | 1015450450 | 20080101 |