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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7788774 | 8163235 | I | 7788774-3 | 20110918 | 20110930 | EXP | JP-ELI_LILLY_AND_COMPANY-JP201109006115 | ELI LILLY AND COMPANY | YR | F | Y | 20110929 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7788774 | 1017676075 | PS | FORTEO | 1 | SUBCUTANEOUS | 021318 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7788774 | HO |
Reactions reported
Event ID | PT |
---|---|
7788774 | HOSPITALISATION |
7788774 | APTYALISM |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |