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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126462722 | 12646272 | 2 | F | 20160722 | 20160830 | 20160812 | 20160907 | EXP | US-ASTRAZENECA-2016SE81940 | ASTRAZENECA | 22749.00 | DY | M | Y | 81.20000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126462722 | 12646272 | 1 | PS | BRILINTA | TICAGRELOR | 1 | Oral | U | U | FP5102 | 22433 | 90 | MG | TABLET | Q12H | ||||
126462722 | 12646272 | 2 | SS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | U | 0 | 50 | MG | TABLET | BID | ||||||
126462722 | 12646272 | 3 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Oral | 10-32.5 MG TABLET 1 TABLET AS NEEDED EVERY 6 HRS | 0 | TABLET | |||||||||
126462722 | 12646272 | 4 | C | ANTIHISTAMINE | UNSPECIFIED INGREDIENT | 1 | AS NEEDED | 0 | TABLET | ||||||||||
126462722 | 12646272 | 5 | C | XANAX | ALPRAZOLAM | 1 | Oral | 0 | 1 | MG | TABLET | BID | |||||||
126462722 | 12646272 | 6 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | 0 | 80 | MG | TABLET | QD | ||||||||
126462722 | 12646272 | 7 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | 5 | MG | TABLET | QD | ||||||||
126462722 | 12646272 | 8 | C | ASPIRIN. | ASPIRIN | 1 | 0 | 81 | MG | TABLET | QD | ||||||||
126462722 | 12646272 | 9 | C | ATENOLOL. | ATENOLOL | 1 | 0 | 25 | MG | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126462722 | 12646272 | 1 | Acute coronary syndrome |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126462722 | 12646272 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126462722 | 12646272 | Acute myocardial infarction | |
126462722 | 12646272 | Anger | |
126462722 | 12646272 | Arthralgia | |
126462722 | 12646272 | Asthenia | |
126462722 | 12646272 | Chest pain | |
126462722 | 12646272 | Confusional state | |
126462722 | 12646272 | Cough | |
126462722 | 12646272 | Drug dose omission | |
126462722 | 12646272 | Dyspnoea | |
126462722 | 12646272 | Hyperhidrosis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |