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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125850401 | 12585040 | 1 | I | 20160601 | 20160723 | 20160723 | PER | US-ASTRAZENECA-2016SE60134 | ASTRAZENECA | 19.00 | YR | F | Y | 70.30000 | KG | 20160723 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125850401 | 12585040 | 1 | PS | ZOMIG | ZOLMITRIPTAN | 1 | Nasal | U | 21450 | NASAL SPRAY | |||||||||
125850401 | 12585040 | 2 | C | SPRIX | KETOROLAC TROMETHAMINE | 1 | Nasal | 0 | NASAL SPRAY | ||||||||||
125850401 | 12585040 | 3 | C | NSAIDS | UNSPECIFIED INGREDIENT | 1 | 0 | ||||||||||||
125850401 | 12585040 | 4 | C | DIAZEPAM. | DIAZEPAM | 1 | Intravenous (not otherwise specified) | 0 | |||||||||||
125850401 | 12585040 | 5 | C | COMPAZINE | PROCHLORPERAZINE MALEATE | 1 | Intravenous (not otherwise specified) | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125850401 | 12585040 | 2 | Arthralgia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125850401 | 12585040 | Drug hypersensitivity | |
125850401 | 12585040 | Muscle spasms |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125850401 | 12585040 | 1 | 201601 | 0 |