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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120843515 | 12084351 | 5 | F | 2012 | 20160817 | 20160217 | 20160822 | EXP | US-GLAXOSMITHKLINE-US2016018830 | GLAXOSMITHKLINE | 70.89 | YR | F | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120843515 | 12084351 | 1 | PS | VENTOLIN | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | UNK | 4ZP7440 | 20983 | |||||||||
120843515 | 12084351 | 2 | SS | VENTOLIN | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 2 PUFF(S), PRN | MY8G | 20983 | 2 | DF | |||||||
120843515 | 12084351 | 3 | SS | VENTOLIN | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 2 PUFF(S), PRN | PS5G | 20983 | 2 | DF | |||||||
120843515 | 12084351 | 4 | C | ALBUTEROL + IPRATROPIUM | 2 | Respiratory (inhalation) | U | 0 | |||||||||||
120843515 | 12084351 | 5 | C | COMBIVENT | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | U | 0 | |||||||||||
120843515 | 12084351 | 6 | C | STIOLTO RESPIMAT | OLODATEROL HYDROCHLORIDETIOTROPIUM BROMIDE MONOHYDRATE | 1 | U | 0 | |||||||||||
120843515 | 12084351 | 7 | C | XANAX | ALPRAZOLAM | 1 | U | 0 | |||||||||||
120843515 | 12084351 | 8 | C | OXYGEN. | OXYGEN | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
120843515 | 12084351 | 1 | Dyspnoea |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
120843515 | 12084351 | HO |
120843515 | 12084351 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
120843515 | 12084351 | Anal cancer | |
120843515 | 12084351 | Asthma | |
120843515 | 12084351 | Chemotherapy | |
120843515 | 12084351 | Clostridium difficile infection | |
120843515 | 12084351 | Dehydration | |
120843515 | 12084351 | Delirium | |
120843515 | 12084351 | Device use error | |
120843515 | 12084351 | Drug ineffective | |
120843515 | 12084351 | Dyspnoea | |
120843515 | 12084351 | Ill-defined disorder | |
120843515 | 12084351 | Oxygen saturation decreased | |
120843515 | 12084351 | Panic reaction | |
120843515 | 12084351 | Product cleaning inadequate | |
120843515 | 12084351 | Product quality issue | |
120843515 | 12084351 | Radiotherapy | |
120843515 | 12084351 | Staphylococcal infection | |
120843515 | 12084351 | Underdose |
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 |
---|---|---|---|---|---|---|
120843515 | 12084351 | 1 | 2006 | 0 |