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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127230021 | 12723002 | 1 | I | 20151006 | 20160908 | 20160908 | PER | US-AUROBINDO-AUR-APL-2015-09076 | AUROBINDO | 0.00 | M | Y | 0.00000 | 20160908 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127230021 | 12723002 | 1 | PS | Hydrochlorothiazide 25 mg | HYDROCHLOROTHIAZIDE | 1 | Unknown | 25 MG, UNK | U | U | 40780 | 25 | MG | ||||||
| 127230021 | 12723002 | 2 | SS | KETOPROFEN. | KETOPROFEN | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 127230021 | 12723002 | 3 | SS | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Unknown | 25 MG, UNK | U | U | 0 | 25 | MG | ||||||
| 127230021 | 12723002 | 4 | SS | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 10 MG, UNK | U | U | 0 | 10 | MG | ||||||
| 127230021 | 12723002 | 5 | SS | RECLAST | ZOLEDRONIC ACID | 1 | Unknown | 100 MG, UNK | U | U | 0 | 100 | MG | ||||||
| 127230021 | 12723002 | 6 | SS | LYRICA | PREGABALIN | 1 | Unknown | 25 MG, UNK | U | U | 0 | 25 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127230021 | 12723002 | 1 | Product used for unknown indication |
| 127230021 | 12723002 | 2 | Product used for unknown indication |
| 127230021 | 12723002 | 3 | Product used for unknown indication |
| 127230021 | 12723002 | 4 | Product used for unknown indication |
| 127230021 | 12723002 | 5 | Product used for unknown indication |
| 127230021 | 12723002 | 6 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127230021 | 12723002 | Drug hypersensitivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |