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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126351721 | 12635172 | 1 | I | 20160704 | 20160802 | 20160809 | 20160809 | EXP | GB-MHRA-ADR 23580485 | PHFR2016GB006319 | NOVARTIS | 57.00 | YR | M | Y | 0.00000 | 20160809 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126351721 | 12635172 | 1 | PS | ZOLEDRONIC ACID | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | UNK | Y | 21223 | |||||||||
| 126351721 | 12635172 | 2 | C | OMEPRAZOLE SODIUM | OMEPRAZOLE SODIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 3 | C | CARBOCISTEINE | CARBOCYSTEINE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 4 | C | CICLESONIDE | CICLESONIDE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 5 | C | ZOPICLONE | ZOPICLONE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 6 | C | SALMETEROL | SALMETEROL | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 7 | C | SOLPHYLLIN | 2 | Unknown | UNK | U | 0 | ||||||||||
| 126351721 | 12635172 | 8 | C | TIOTROPIUM | TIOTROPIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 9 | C | AZITHROMYCIN ANHYDROUS. | AZITHROMYCIN ANHYDROUS | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 10 | C | COCODAMOL | ACETAMINOPHENCODEINE PHOSPHATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 11 | C | SALBUTAMOL | ALBUTEROL | 1 | Unknown | UNK | U | 0 | |||||||||
| 126351721 | 12635172 | 12 | C | ZAFIRLUKAST. | ZAFIRLUKAST | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126351721 | 12635172 | 1 | Product used for unknown indication |
| 126351721 | 12635172 | 2 | Product used for unknown indication |
| 126351721 | 12635172 | 3 | Product used for unknown indication |
| 126351721 | 12635172 | 4 | Product used for unknown indication |
| 126351721 | 12635172 | 5 | Product used for unknown indication |
| 126351721 | 12635172 | 6 | Product used for unknown indication |
| 126351721 | 12635172 | 7 | Product used for unknown indication |
| 126351721 | 12635172 | 8 | Product used for unknown indication |
| 126351721 | 12635172 | 9 | Product used for unknown indication |
| 126351721 | 12635172 | 10 | Product used for unknown indication |
| 126351721 | 12635172 | 11 | Product used for unknown indication |
| 126351721 | 12635172 | 12 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126351721 | 12635172 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126351721 | 12635172 | Chronic obstructive pulmonary disease | |
| 126351721 | 12635172 | Dyspnoea | |
| 126351721 | 12635172 | Hypersensitivity | |
| 126351721 | 12635172 | Malaise | |
| 126351721 | 12635172 | Nausea | |
| 126351721 | 12635172 | Pain | |
| 126351721 | 12635172 | Rash |
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 |
|---|---|---|---|---|---|---|
| 126351721 | 12635172 | 1 | 20160704 | 20160704 | 0 |