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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126561271 | 12656127 | 1 | I | 201608 | 20160812 | 20160816 | 20160816 | PER | US-BAYER-2016-157726 | BAYER | 78.00 | YR | E | F | Y | 50.80000 | KG | 20160816 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126561271 | 12656127 | 1 | PS | CLARITIN-D 12 HOUR | LORATADINEPSEUDOEPHEDRINE SULFATE | 1 | Oral | 1 DF, QD | Y | CVM05N8 | 19670 | 1 | DF | PROLONGED-RELEASE TABLET | QD | ||||
126561271 | 12656127 | 2 | C | ASPIRIN. | ASPIRIN | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 3 | C | STATIN | UNSPECIFIED INGREDIENT | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 4 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 5 | C | LOVAZA | OMEGA-3-ACID ETHYL ESTERS | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 6 | C | VASOGEN | 2 | 0 | |||||||||||||
126561271 | 12656127 | 7 | C | COQ10 | UBIDECARENONE | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 8 | C | CALCIUM | CALCIUM | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 9 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 10 | C | VITAMIN C | ASCORBIC ACID | 1 | 0 | ||||||||||||
126561271 | 12656127 | 11 | C | LUTEIN | LUTEIN | 1 | 0 | ||||||||||||
126561271 | 12656127 | 12 | C | MULTIVITAMIN | VITAMINS | 1 | UNK | 0 | |||||||||||
126561271 | 12656127 | 13 | C | MAGNESIUM | MAGNESIUM | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126561271 | 12656127 | 1 | Upper-airway cough syndrome |
126561271 | 12656127 | 2 | Ischaemic heart disease prophylaxis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126561271 | 12656127 | Drug prescribing error | |
126561271 | 12656127 | Insomnia | |
126561271 | 12656127 | Product use issue |
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 |
---|---|---|---|---|---|---|
126561271 | 12656127 | 1 | 20160808 | 20160811 | 0 |