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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4463176 | 4219137 | I | 4463176-6 | 20040923 | 20040930 | EXP | PHBS2004BR12749 | NOVARTIS PHARMACEUTICALS CORP. | 48 | YR | F | Y | 20040930 | MD |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4463176 | 1005252395 | PS | SANDOSTATIN LAR | 1 | INTRAMUSCULAR |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4463176 | 1005252395 | ACROMEGALY |
Outcome of event
Event ID | OUTC COD |
---|---|
4463176 | OT |
Reactions reported
Event ID | PT |
---|---|
4463176 | ERYTHEMA MULTIFORME |
4463176 | INJECTION SITE REACTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |