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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7387282 | 7880421 | I | 7387282-1 | 20110316 | 20110331 | PER | US-CUBIST-2011S1000008 | CUBIST PHARMACEUTICALS, INC. | YR | Y | 20110331 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7387282 | 1016141322 | PS | CUBICIN | 1 | UNKNOWN | 021572 | |||||
7387282 | 1016141323 | SS | CUBICIN | 1 | UNKNOWN | 021572 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7387282 | 1016141322 | CELLULITIS |
7387282 | 1016141323 | ABSCESS |
Outcome of event
Event ID | OUTC COD |
---|---|
7387282 | OT |
Reactions reported
Event ID | PT |
---|---|
7387282 | PANCYTOPENIA |
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 |
---|---|---|---|---|---|
7387282 | 1016141322 | 5 | DAY | ||
7387282 | 1016141323 | 5 | DAY |