Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127654981 | 12765498 | 1 | I | 2015 | 20160912 | 20160921 | 20160921 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201609004393 | ELI LILLY AND CO | 0.00 | F | Y | 50.00000 | KG | 20160920 | CN | BR | BR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127654981 | 12765498 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Unknown | 20 UG, QD | 21318 | 20 | UG | INJECTION | QD | ||||||
| 127654981 | 12765498 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | 0 | CAPSULE | |||||||||
| 127654981 | 12765498 | 3 | C | AZULFIDINE | SULFASALAZINE | 1 | UNK, UNKNOWN | 0 | |||||||||||
| 127654981 | 12765498 | 4 | C | METOTREXATO /00113801/ | METHOTREXATE | 1 | UNK, UNKNOWN | 0 | |||||||||||
| 127654981 | 12765498 | 5 | C | NORTRIPTILINA | 2 | 25 MG, UNKNOWN | 0 | 25 | MG | ||||||||||
| 127654981 | 12765498 | 6 | C | CALCIUM | CALCIUM | 1 | UNK, UNKNOWN | 0 | |||||||||||
| 127654981 | 12765498 | 7 | C | OMEPRAZOL /00661201/ | OMEPRAZOLE | 1 | UNK, UNKNOWN | 0 | |||||||||||
| 127654981 | 12765498 | 8 | C | ARTROLIVE | CHONDROITIN SULFATE (BOVINE)GLUCOSAMINE SULFATE | 1 | UNK, UNKNOWN | 0 | |||||||||||
| 127654981 | 12765498 | 9 | C | ACIDO FOLICO /00024201/ | FOLIC ACID | 1 | UNK, UNKNOWN | 0 | |||||||||||
| 127654981 | 12765498 | 10 | C | AD TIL | 2 | UNK, UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127654981 | 12765498 | 1 | Osteoporosis |
| 127654981 | 12765498 | 2 | Pain |
| 127654981 | 12765498 | 3 | Product used for unknown indication |
| 127654981 | 12765498 | 4 | Product used for unknown indication |
| 127654981 | 12765498 | 5 | Insomnia |
| 127654981 | 12765498 | 6 | Product used for unknown indication |
| 127654981 | 12765498 | 7 | Product used for unknown indication |
| 127654981 | 12765498 | 8 | Product used for unknown indication |
| 127654981 | 12765498 | 9 | Product used for unknown indication |
| 127654981 | 12765498 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127654981 | 12765498 | HO |
| 127654981 | 12765498 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127654981 | 12765498 | Arrhythmia | |
| 127654981 | 12765498 | Arthralgia | |
| 127654981 | 12765498 | Blood pressure increased | |
| 127654981 | 12765498 | Constipation | |
| 127654981 | 12765498 | Depression | |
| 127654981 | 12765498 | Drug administered at inappropriate site | |
| 127654981 | 12765498 | Feeding disorder | |
| 127654981 | 12765498 | Femur fracture | |
| 127654981 | 12765498 | Gait disturbance | |
| 127654981 | 12765498 | Injection site bruising | |
| 127654981 | 12765498 | Injection site haemorrhage | |
| 127654981 | 12765498 | Injection site mass | |
| 127654981 | 12765498 | Insomnia | |
| 127654981 | 12765498 | Ischaemic stroke | |
| 127654981 | 12765498 | Nausea | |
| 127654981 | 12765498 | Oral disorder | |
| 127654981 | 12765498 | Syncope | |
| 127654981 | 12765498 | Visual impairment | |
| 127654981 | 12765498 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127654981 | 12765498 | 1 | 201604 | 0 |