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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
76267735 | 7626773 | 5 | F | 200912 | 20160630 | 20101013 | 20160927 | PER | US-ASTRAZENECA-2010SE22945 | ASTRAZENECA | 703.00 | MON | F | Y | 81.60000 | KG | 20160927 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
76267735 | 7626773 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/ 4.5 MCG, TWO INHALATIONS TWICE DAILY | 3001092C00 | 21929 | |||||||||
76267735 | 7626773 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/ 4.5 MCG, TWO INHALATIONS TWICE DAILY | 3001092C00 | 21929 | |||||||||
76267735 | 7626773 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/ 4.5 MCG, 2 PUFFS TWICE A DAY, | 3001195C00 | 21929 | |||||||||
76267735 | 7626773 | 4 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/ 4.5 MCG, 2 PUFFS TWICE A DAY, | 3001195C00 | 21929 | |||||||||
76267735 | 7626773 | 5 | C | LITHIUM. | LITHIUM | 1 | 0 | 1200 | MG | QD | |||||||||
76267735 | 7626773 | 6 | C | LITHIUM. | LITHIUM | 1 | 0 | 300 | MG | BID | |||||||||
76267735 | 7626773 | 7 | C | NAVANE | THIOTHIXENE | 1 | 0 | 4 | MG | QD | |||||||||
76267735 | 7626773 | 8 | C | RISPERDAL | RISPERIDONE | 1 | 0 | 2 | MG | QD | |||||||||
76267735 | 7626773 | 9 | C | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | TWO TIMES A DAY | 0 | |||||||||||
76267735 | 7626773 | 10 | C | CELEXA | CITALOPRAM HYDROBROMIDE | 1 | 0 | 20 | MG | QD | |||||||||
76267735 | 7626773 | 11 | C | OXYGEN. | OXYGEN | 1 | Nasal | 0 | 1.5 | L | QD | ||||||||
76267735 | 7626773 | 12 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 0 | |||||||||||
76267735 | 7626773 | 13 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Respiratory (inhalation) | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
76267735 | 7626773 | 1 | Chronic obstructive pulmonary disease |
76267735 | 7626773 | 2 | Emphysema |
76267735 | 7626773 | 3 | Chronic obstructive pulmonary disease |
76267735 | 7626773 | 4 | Emphysema |
76267735 | 7626773 | 11 | Dyspnoea |
76267735 | 7626773 | 12 | Supplementation therapy |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
76267735 | 7626773 | Chills | |
76267735 | 7626773 | Circumstance or information capable of leading to medication error | |
76267735 | 7626773 | Drug dose omission | |
76267735 | 7626773 | Dyspnoea | |
76267735 | 7626773 | Fatigue | |
76267735 | 7626773 | Feeling cold | |
76267735 | 7626773 | Intentional device misuse | |
76267735 | 7626773 | Panic reaction | |
76267735 | 7626773 | Product quality 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 |
---|---|---|---|---|---|---|
76267735 | 7626773 | 1 | 200912 | 0 | ||
76267735 | 7626773 | 2 | 200912 | 0 | ||
76267735 | 7626773 | 3 | 200912 | 0 | ||
76267735 | 7626773 | 4 | 200912 | 0 |