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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127247651 | 12724765 | 1 | I | 20151229 | 20160908 | 20160908 | PER | US-DRREDDYS-USA/USA/15/0055135 | DR REDDYS | 0.00 | F | Y | 97.50000 | KG | 20160908 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127247651 | 12724765 | 1 | PS | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | Y | U | UNKNOWN | 91650 | ||||||||
| 127247651 | 12724765 | 2 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | 0 | 100 | MG | QD | ||||||||
| 127247651 | 12724765 | 3 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 0 | 20 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127247651 | 12724765 | 1 | Blood cholesterol increased |
| 127247651 | 12724765 | 2 | Thyroid disorder |
| 127247651 | 12724765 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127247651 | 12724765 | Arthralgia | |
| 127247651 | 12724765 | Drug ineffective | |
| 127247651 | 12724765 | Product quality issue |
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 |
|---|---|---|---|---|---|---|
| 127247651 | 12724765 | 1 | 201306 | 20150526 | 0 |