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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126805102 | 12680510 | 2 | F | 20160714 | 20160818 | 20160824 | 20160824 | EXP | PHHY2016FR114137 | SANDOZ | 72.56 | YR | M | Y | 0.00000 | 20160825 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126805102 | 12680510 | 1 | SS | ONBREZ BREEZHALER | INDACATEROL | 1 | Respiratory (inhalation) | 150 UG, UNK | Y | 0 | 150 | UG | DRY POWDER INHALER | ||||||
126805102 | 12680510 | 2 | PS | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 100 MG, QD | Y | 70268 | 100 | MG | QD | ||||||
126805102 | 12680510 | 3 | SS | SOTALOL. | SOTALOL | 1 | Oral | 80 MG, QD | Y | 0 | 80 | MG | QD | ||||||
126805102 | 12680510 | 4 | SS | AMIODARONE | AMIODARONE | 1 | Oral | 200 MG, QD | Y | 0 | 200 | MG | QD | ||||||
126805102 | 12680510 | 5 | SS | PREVISCAN | FLUINDIONE | 1 | Oral | UNK | Y | 0 | |||||||||
126805102 | 12680510 | 6 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | UNK | 0 | ||||||||||
126805102 | 12680510 | 7 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126805102 | 12680510 | 1 | Chronic obstructive pulmonary disease |
126805102 | 12680510 | 2 | Product used for unknown indication |
126805102 | 12680510 | 3 | Hypertension |
126805102 | 12680510 | 4 | Atrial fibrillation |
126805102 | 12680510 | 5 | Thrombosis prophylaxis |
126805102 | 12680510 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126805102 | 12680510 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126805102 | 12680510 | Liver injury | |
126805102 | 12680510 | Lung disorder |
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 |
---|---|---|---|---|---|---|
126805102 | 12680510 | 1 | 20160727 | 0 | ||
126805102 | 12680510 | 2 | 20160727 | 0 | ||
126805102 | 12680510 | 3 | 201308 | 20160717 | 0 | |
126805102 | 12680510 | 4 | 201311 | 20160717 | 0 | |
126805102 | 12680510 | 5 | 2011 | 20160717 | 0 | |
126805102 | 12680510 | 6 | 20160727 | 0 | ||
126805102 | 12680510 | 7 | 20160803 | 0 |