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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5577899 | 6517134 | I | 5577899-9 | 20071201 | 20071218 | 20071231 | EXP | ES-ELI_LILLY_AND_COMPANY-ES200712003826 | ELI LILLY AND COMPANY | 69 | YR | F | Y | 20071221 | CN | SPAIN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5577899 | 1009350011 | PS | FORTEO | 1 | SUBCUTANEOUS | 20 UG, UNKNOWN | 021318 | ||||
5577899 | 1009350012 | C | ADIRO | 2 | UNKNOWN | UNK, UNKNOWN | |||||
5577899 | 1009350013 | C | CITALOPRAM HYDROBROMIDE | 1 | UNKNOWN | UNK, UNKNOWN | |||||
5577899 | 1009350014 | C | ANTIBIOTICS | 2 | UNKNOWN | UNK, UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5577899 | 1009350011 | OSTEOPOROSIS |
5577899 | 1009350012 | PLATELET COUNT INCREASED |
5577899 | 1009350014 | EAR INFECTION |
Outcome of event
Event ID | OUTC COD |
---|---|
5577899 | HO |
Reactions reported
Event ID | PT |
---|---|
5577899 | ASTHENIA |
5577899 | BEDRIDDEN |
5577899 | DIARRHOEA |
5577899 | FALL |
5577899 | PLEURAL EFFUSION |
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 |
---|---|---|---|---|---|
5577899 | 1009350011 | 20070301 |