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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127686461 | 12768646 | 1 | I | 20081116 | 20160907 | 20160921 | 20160921 | EXP | US-AMNEAL PHARMACEUTICALS-2016AMN00522 | AMNEAL | 86.00 | YR | M | Y | 94.00000 | KG | 20160921 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127686461 | 12768646 | 1 | PS | NAPROXEN. | NAPROXEN | 1 | Oral | UNK | U | 75927 | |||||||||
| 127686461 | 12768646 | 2 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 20 MG, 1X/DAY | 4320 | MG | U | 0 | 20 | MG | CAPSULE | QD | |||
| 127686461 | 12768646 | 3 | C | ATENOLOL. | ATENOLOL | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 4 | C | NORVASC | AMLODIPINE BESYLATE | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 5 | C | tamsulosin | TAMSULOSIN | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 6 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 7 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 8 | C | VESICARE | SOLIFENACIN SUCCINATE | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 9 | C | ASA | ASPIRIN | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 10 | C | multivitamins | VITAMINS | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 11 | C | calcium with Vit D | 2 | Oral | UNK | 0 | |||||||||||
| 127686461 | 12768646 | 12 | C | chondroitin/glucosamine | CHONDROITIN SULFATE (BOVINE)GLUCOSAMINE SULFATE | 1 | Oral | UNK | 0 | ||||||||||
| 127686461 | 12768646 | 13 | C | OCUVITE | VITAMINS | 1 | Oral | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127686461 | 12768646 | 1 | Osteoarthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127686461 | 12768646 | HO |
| 127686461 | 12768646 | DE |
| 127686461 | 12768646 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127686461 | 12768646 | Myocardial infarction |
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 |
|---|---|---|---|---|---|---|
| 127686461 | 12768646 | 1 | 20080415 | 20081116 | 0 | |
| 127686461 | 12768646 | 2 | 20080415 | 20081116 | 0 | |
| 127686461 | 12768646 | 3 | 2006 | 20081116 | 0 | |
| 127686461 | 12768646 | 4 | 20080327 | 20081116 | 0 | |
| 127686461 | 12768646 | 5 | 20080801 | 20081116 | 0 | |
| 127686461 | 12768646 | 6 | 20080811 | 20081116 | 0 | |
| 127686461 | 12768646 | 7 | 2006 | 20081116 | 0 | |
| 127686461 | 12768646 | 8 | 20080801 | 20081111 | 0 | |
| 127686461 | 12768646 | 9 | 2006 | 20081116 | 0 | |
| 127686461 | 12768646 | 10 | 1998 | 20081116 | 0 | |
| 127686461 | 12768646 | 11 | 2003 | 20081116 | 0 | |
| 127686461 | 12768646 | 12 | 2003 | 20081116 | 0 | |
| 127686461 | 12768646 | 13 | 20080301 | 20081116 | 0 |