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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127542781 | 12754278 | 1 | I | 201604 | 20160516 | 20160916 | 20160916 | PER | US-ASTRAZENECA-2016SE53289 | ASTRAZENECA | 71.00 | YR | F | Y | 0.00000 | 20160916 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127542781 | 12754278 | 1 | PS | PRILOSEC OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 21229 | 2 | DF | MODIFIED-RELEASE TABLET | QD | |||||||
127542781 | 12754278 | 2 | SS | PRILOSEC OTC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 6083171972 | 21229 | MODIFIED-RELEASE TABLET | |||||||||
127542781 | 12754278 | 3 | C | FISH OIL | FISH OIL | 1 | 0 | ||||||||||||
127542781 | 12754278 | 4 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127542781 | 12754278 | Arthralgia | |
127542781 | 12754278 | Arthropathy | |
127542781 | 12754278 | Dizziness | |
127542781 | 12754278 | Dizziness postural | |
127542781 | 12754278 | Dyspnoea | |
127542781 | 12754278 | Headache | |
127542781 | 12754278 | Hypoaesthesia | |
127542781 | 12754278 | Lethargy | |
127542781 | 12754278 | Muscular weakness | |
127542781 | 12754278 | Myalgia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |