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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7387536 | 7880612 | I | 7387536-9 | 20080922 | 20110323 | 20110331 | EXP | JP-PFIZER INC-2011063718 | PFIZERINC | 84 | YR | F | Y | 20110330 | MD | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7387536 | 1016142575 | PS | METHYLPREDNISOLONE SODIUM SUCCINATE | 2 | INTRAVENOUS DRIP | 500MG/DAY | 011153 | ||||
7387536 | 1016142576 | C | PREDNISOLONE | 2 | ORAL | UNK | |||||
7387536 | 1016142578 | C | PREDNISOLONE | 2 | UNK | ||||||
7387536 | 1016142577 | C | PREDNISOLONE | 2 | UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7387536 | 1016142575 | PEMPHIGUS |
7387536 | 1016142576 | PEMPHIGUS |
Outcome of event
Event ID | OUTC COD |
---|---|
7387536 | OT |
Reactions reported
Event ID | PT |
---|---|
7387536 | DISSEMINATED INTRAVASCULAR COAGULATION |
7387536 | PULMONARY ARTERY THROMBOSIS |
7387536 | VENOUS THROMBOSIS |
7387536 | SEPSIS |
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 |
---|---|---|---|---|---|
7387536 | 1016142575 | 20080910 | 20080912 | 3 | DAY |
7387536 | 1016142576 | 20080101 | |||
7387536 | 1016142577 | 20080101 |