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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123835202 | 12383520 | 2 | F | 201106 | 20160808 | 20160518 | 20160812 | EXP | US-DSJP-DSU-2016-116248 | DAIICHI | 0.00 | Y | 0.00000 | 20160812 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123835202 | 12383520 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/25 MG, UNK | U | 21532 | 1 | DF | FILM-COATED TABLET | |||||||
123835202 | 12383520 | 2 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
123835202 | 12383520 | 3 | C | AMLODIPINE BESYLATE. | AMLODIPINE BESYLATE | 1 | UNK | 0 | |||||||||||
123835202 | 12383520 | 4 | C | METOPROLOL. | METOPROLOL | 1 | UNK | 0 | |||||||||||
123835202 | 12383520 | 5 | C | VITAMIN D /00107901/ | ERGOCALCIFEROL | 1 | UNK | 0 | |||||||||||
123835202 | 12383520 | 6 | C | NASACORT | TRIAMCINOLONE ACETONIDE | 1 | UNK | 0 | |||||||||||
123835202 | 12383520 | 7 | C | EXCEDRIN | ACETAMINOPHENASPIRINCAFFEINE | 1 | 0 | ||||||||||||
123835202 | 12383520 | 8 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123835202 | 12383520 | 1 | Hypertension |
123835202 | 12383520 | 2 | Product used for unknown indication |
123835202 | 12383520 | 3 | Product used for unknown indication |
123835202 | 12383520 | 4 | Product used for unknown indication |
123835202 | 12383520 | 5 | Product used for unknown indication |
123835202 | 12383520 | 6 | Product used for unknown indication |
123835202 | 12383520 | 7 | Product used for unknown indication |
123835202 | 12383520 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123835202 | 12383520 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123835202 | 12383520 | Anxiety | |
123835202 | 12383520 | Dizziness | |
123835202 | 12383520 | Malabsorption |
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 |
---|---|---|---|---|---|---|
123835202 | 12383520 | 1 | 20090430 | 201507 | 0 |