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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126746211 | 12674621 | 1 | I | 20150907 | 20150908 | 20160822 | 20160822 | PER | US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-07955-2015 | RECKITT BENCKISER | 0.00 | A | M | Y | 0.00000 | 20160822 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126746211 | 12674621 | 1 | PS | MUCINEX | GUAIFENESIN | 1 | Unknown | 2 DF, BID | U | U | 0 | 2 | DF |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126746211 | 12674621 | 1 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126746211 | 12674621 | Abdominal pain | |
126746211 | 12674621 | Accidental overdose | |
126746211 | 12674621 | Diarrhoea | |
126746211 | 12674621 | Dizziness | |
126746211 | 12674621 | Skin odour abnormal |
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 |
---|---|---|---|---|---|---|
126746211 | 12674621 | 1 | 20150907 | 0 |