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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127191761 | 12719176 | 1 | I | 2016 | 20160622 | 20160907 | 20160907 | PER | US-JNJFOC-20160621190 | JANSSEN | 0.00 | A | F | Y | 88.45000 | KG | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127191761 | 12719176 | 1 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | N | UNKNOWN | 19813 | UNSPECIFIED | ||||||||
| 127191761 | 12719176 | 2 | C | LANTUS | INSULIN GLARGINE | 1 | Unknown | 18 MG IN MORNING AND 28 MG AT NIGHT | 0 | UNSPECIFIED | |||||||||
| 127191761 | 12719176 | 3 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | 0 | 500 | MG | UNSPECIFIED | BID | |||||||
| 127191761 | 12719176 | 4 | C | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Unknown | 0 | 225 | MG | UNSPECIFIED | ||||||||
| 127191761 | 12719176 | 5 | C | GLYBURIDE. | GLYBURIDE | 1 | Unknown | 0 | 5 | MG | UNSPECIFIED | BID | |||||||
| 127191761 | 12719176 | 6 | C | FENOFIBRATE. | FENOFIBRATE | 1 | Unknown | 0 | 145 | MG | UNSPECIFIED | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127191761 | 12719176 | 1 | Back pain |
| 127191761 | 12719176 | 2 | Type 2 diabetes mellitus |
| 127191761 | 12719176 | 3 | Type 2 diabetes mellitus |
| 127191761 | 12719176 | 4 | Blood cholesterol increased |
| 127191761 | 12719176 | 5 | Type 2 diabetes mellitus |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127191761 | 12719176 | Hyperhidrosis | |
| 127191761 | 12719176 | Product adhesion issue | |
| 127191761 | 12719176 | Underdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |