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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127191911 | 12719191 | 1 | I | 20160720 | 20160907 | 20160907 | PER | US-JNJFOC-20160716976 | JANSSEN | 0.00 | A | F | Y | 54.43000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127191911 | 12719191 | 1 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | N | N | UNKNOWN;1509824P1 | 0 | MATRIX PATCH | |||||||
| 127191911 | 12719191 | 2 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | N | N | UNKNOWN;1509824P1 | 19813 | MATRIX PATCH | |||||||
| 127191911 | 12719191 | 3 | C | SUMATRIPTAN. | SUMATRIPTAN | 1 | Subcutaneous | AS NEEDED | 0 | .5 | ML | SOLUTION | QD | ||||||
| 127191911 | 12719191 | 4 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Oral | 0 | 40 | MG | UNSPECIFIED | QD | |||||||
| 127191911 | 12719191 | 5 | C | GABAPENTIN. | GABAPENTIN | 1 | Oral | 0 | 200 | MG | CAPSULE | TID | |||||||
| 127191911 | 12719191 | 6 | C | CYCLOBENZAPRIN | CYCLOBENZAPRINE | 1 | Oral | 0 | 10 | MG | CAPSULE | BID | |||||||
| 127191911 | 12719191 | 7 | C | LORAZEPAM. | LORAZEPAM | 1 | Oral | AS NEEDED | 0 | .5 | MG | UNSPECIFIED | BID | ||||||
| 127191911 | 12719191 | 8 | C | MIRTAZAPINE. | MIRTAZAPINE | 1 | Oral | AS NEEDED | 0 | 45 | MG | UNSPECIFIED | QD | ||||||
| 127191911 | 12719191 | 9 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Respiratory (inhalation) | AS NEEDED | 0 | CAPSULE | |||||||||
| 127191911 | 12719191 | 10 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Unknown | AS NEEDED | 0 | .5 | ML | UNSPECIFIED | TID | ||||||
| 127191911 | 12719191 | 11 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | AS NEEDED | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127191911 | 12719191 | 1 | Pain |
| 127191911 | 12719191 | 2 | Pain |
| 127191911 | 12719191 | 3 | Migraine |
| 127191911 | 12719191 | 4 | Gastric disorder |
| 127191911 | 12719191 | 5 | Product used for unknown indication |
| 127191911 | 12719191 | 6 | Product used for unknown indication |
| 127191911 | 12719191 | 7 | Product used for unknown indication |
| 127191911 | 12719191 | 8 | Product used for unknown indication |
| 127191911 | 12719191 | 9 | Product used for unknown indication |
| 127191911 | 12719191 | 10 | Product used for unknown indication |
| 127191911 | 12719191 | 11 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127191911 | 12719191 | Drug ineffective | |
| 127191911 | 12719191 | Inappropriate schedule of drug administration | |
| 127191911 | 12719191 | Product quality issue | |
| 127191911 | 12719191 | Underdose | |
| 127191911 | 12719191 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |