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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125663531 | 12566353 | 1 | I | 20150709 | 20160718 | 20160718 | PER | US-IGI LABORATORIES, INC.-1055194 | IGI LABORATORIES | 0.00 | F | Y | 0.00000 | 20160718 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125663531 | 12566353 | 1 | PS | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | Unknown | U | 19090 | ||||||||||
125663531 | 12566353 | 2 | SS | ZEGERID | OMEPRAZOLESODIUM BICARBONATE | 1 | Unknown | U | 0 | ||||||||||
125663531 | 12566353 | 3 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | U | 0 | |||||||||||
125663531 | 12566353 | 4 | SS | NEXIUM 24HR | ESOMEPRAZOLE MAGNESIUM | 1 | U | 0 | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125663531 | 12566353 | 1 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125663531 | 12566353 | Depressed mood | |
125663531 | 12566353 | Drug ineffective | |
125663531 | 12566353 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |