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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126350891 | 12635089 | 1 | I | 201209 | 20160727 | 20160808 | 20160808 | EXP | FR-ELI_LILLY_AND_COMPANY-FR201607012069 | ELI LILLY AND CO | 39.00 | YR | F | Y | 0.00000 | 20160808 | CN | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126350891 | 12635089 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | 60 MG, QD | Y | 21427 | 60 | MG | CAPSULE | QD | |||||
| 126350891 | 12635089 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | 30 MG, QD | Y | 21427 | 30 | MG | CAPSULE | QD | |||||
| 126350891 | 12635089 | 3 | SS | LYRICA | PREGABALIN | 1 | Unknown | 500 MG, QD | Y | U | 0 | 500 | MG | QD | |||||
| 126350891 | 12635089 | 4 | SS | LYRICA | PREGABALIN | 1 | Unknown | 100 MG, QD | Y | U | 0 | 100 | MG | QD | |||||
| 126350891 | 12635089 | 5 | C | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | Unknown | 200 MG, QD | 0 | 200 | MG | QD | |||||||
| 126350891 | 12635089 | 6 | C | IXPRIM | ACETAMINOPHENTRAMADOL HYDROCHLORIDE | 1 | Unknown | UNK UNK, OTHER | U | U | 0 | ||||||||
| 126350891 | 12635089 | 7 | C | XANAX | ALPRAZOLAM | 1 | Unknown | 0.5 MG, TID | U | U | 0 | .5 | MG | TID | |||||
| 126350891 | 12635089 | 8 | C | VOLTAREN | DICLOFENAC SODIUM | 1 | Unknown | UNK UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126350891 | 12635089 | 1 | Product used for unknown indication |
| 126350891 | 12635089 | 3 | Product used for unknown indication |
| 126350891 | 12635089 | 5 | Product used for unknown indication |
| 126350891 | 12635089 | 6 | Product used for unknown indication |
| 126350891 | 12635089 | 7 | Product used for unknown indication |
| 126350891 | 12635089 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126350891 | 12635089 | OT |
| 126350891 | 12635089 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126350891 | 12635089 | Asthenia | |
| 126350891 | 12635089 | Chest pain | |
| 126350891 | 12635089 | Congestive cardiomyopathy | |
| 126350891 | 12635089 | Dyspnoea | |
| 126350891 | 12635089 | Ejection fraction abnormal | |
| 126350891 | 12635089 | Electrocardiogram ST segment elevation | |
| 126350891 | 12635089 | Hyperhidrosis | |
| 126350891 | 12635089 | Pain | |
| 126350891 | 12635089 | Sinus tachycardia |
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 |
|---|---|---|---|---|---|---|
| 126350891 | 12635089 | 2 | 2012 | 0 | ||
| 126350891 | 12635089 | 4 | 2012 | 0 | ||
| 126350891 | 12635089 | 5 | 201203 | 0 |