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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124750552 | 12475055 | 2 | F | 201508 | 20160706 | 20160617 | 20160714 | EXP | US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-07573-2015 | RECKITT BENCKISER | 87.34 | YR | F | Y | 46.30000 | KG | 20160714 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124750552 | 12475055 | 1 | PS | MUCINEX | GUAIFENESIN | 1 | Unknown | 20 ML, EVERY 4 HOURS | N | U | 5121E1 | 0 | 20 | ML | ORAL LIQUID | ||||
124750552 | 12475055 | 2 | C | MINERAL | 2 | Unknown | UNK | U | 0 | ||||||||||
124750552 | 12475055 | 3 | C | ESTER-C /00008001/ | 2 | Oral | 1000 MG, QD | U | 0 | 1000 | MG | TABLET | |||||||
124750552 | 12475055 | 4 | C | ZINC | ZINCINC CHLORIDE | 1 | Oral | 100 MG, QD | U | 0 | 100 | MG | TABLET | ||||||
124750552 | 12475055 | 5 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 400 MCG, EVERY DAY | U | 0 | TABLET | ||||||||
124750552 | 12475055 | 6 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | Unknown | UNK | U | 0 | CAPSULE | ||||||||
124750552 | 12475055 | 7 | C | CHROMIUM | CHROMIC CHLORIDECHROMIUM | 1 | Oral | 200 MCG, QD | U | 0 | TABLET | ||||||||
124750552 | 12475055 | 8 | C | VITAMIN C | ASCORBIC ACID | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124750552 | 12475055 | 1 | Cough |
124750552 | 12475055 | 2 | Product used for unknown indication |
124750552 | 12475055 | 3 | Product used for unknown indication |
124750552 | 12475055 | 4 | Product used for unknown indication |
124750552 | 12475055 | 5 | Product used for unknown indication |
124750552 | 12475055 | 6 | Product used for unknown indication |
124750552 | 12475055 | 7 | Product used for unknown indication |
124750552 | 12475055 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124750552 | 12475055 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124750552 | 12475055 | Accelerated hypertension | |
124750552 | 12475055 | Burning sensation | |
124750552 | 12475055 | Dermatitis allergic | |
124750552 | 12475055 | Drug ineffective | |
124750552 | 12475055 | Insomnia | |
124750552 | 12475055 | Pruritus | |
124750552 | 12475055 | Rash | |
124750552 | 12475055 | Rash pruritic | |
124750552 | 12475055 | Urticaria |
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 |
---|---|---|---|---|---|---|
124750552 | 12475055 | 1 | 20150823 | 20150824 | 0 | |
124750552 | 12475055 | 3 | 20090729 | 0 | ||
124750552 | 12475055 | 4 | 20090729 | 0 | ||
124750552 | 12475055 | 5 | 20090729 | 0 | ||
124750552 | 12475055 | 6 | 20110309 | 0 | ||
124750552 | 12475055 | 7 | 20110504 | 0 |