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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126392281 | 12639228 | 1 | I | 2013 | 20160614 | 20160810 | 20160810 | PER | US-ASTRAZENECA-2016SE66209 | ASTRAZENECA | 62.00 | YR | F | Y | 59.00000 | KG | 20160810 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126392281 | 12639228 | 1 | PS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | Y | U | 0 | |||||||||
126392281 | 12639228 | 2 | SS | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Oral | UNK | 0 | 30 | MG | CAPSULE | QD | ||||||
126392281 | 12639228 | 3 | SS | UNKNOWN MEDICATION | UNSPECIFIED INGREDIENT | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126392281 | 12639228 | 1 | Gastrooesophageal reflux disease |
126392281 | 12639228 | 2 | Gastrooesophageal reflux disease |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126392281 | 12639228 | Ankle fracture | |
126392281 | 12639228 | Blood sodium decreased | |
126392281 | 12639228 | Diarrhoea | |
126392281 | 12639228 | Dyspepsia | |
126392281 | 12639228 | Dysstasia | |
126392281 | 12639228 | Feeling abnormal | |
126392281 | 12639228 | Pollakiuria | |
126392281 | 12639228 | Somnolence |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |