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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125807064 | 12580706 | 4 | F | 20160530 | 20160725 | 20160721 | 20160902 | EXP | GB-ACTAVIS-2016-15871 | ACTAVIS | 71.00 | YR | M | Y | 0.00000 | 20160902 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125807064 | 12580706 | 1 | SS | ASPIRIN. | ASPIRIN | 1 | Unknown | 75 MG, DAILY | U | UNCONFIRMED | 0 | 75 | MG | QD | |||||
| 125807064 | 12580706 | 2 | SS | Carbocisteine (Unknown) | CARBOCYSTEINE | 1 | Unknown | 750 MG, DAILY | U | UNCONFIRMED | 0 | 750 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 3 | SS | Diltiazem (Unknown) | DILTIAZEM | 1 | Unknown | 180 MG, DAILY | U | UNCONFIRMED | 0 | 180 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 4 | SS | FERROUS SULFATE. | FERROUS SULFATE | 1 | Unknown | UNK | U | UNCONFIRMED | 0 | UNK | |||||||
| 125807064 | 12580706 | 5 | SS | Gliclazide (Unknown) | GLICLAZIDE | 1 | Unknown | 80 MG, DAILY | U | UNCONFIRMED | 0 | 80 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 6 | SS | Ipratropium (Unknown) | IPRATROPIUM | 1 | Unknown | 500 MG, DAILY | U | UNCONFIRMED | 0 | 500 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 7 | SS | Itraconazole (Unknown) | ITRACONAZOLE | 1 | Unknown | 200 MG, DAILY | U | UNCONFIRMED | 0 | 200 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 8 | PS | Lansoprazole (Unknown) | LANSOPRAZOLE | 1 | Unknown | 30 MG, DAILY | U | UNCONFIRMED | 203306 | 30 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 9 | SS | Metformin (Unknown) | METFORMIN HYDROCHLORIDE | 1 | Unknown | UNK | U | UNCONFIRMED | 0 | UNK | |||||||
| 125807064 | 12580706 | 10 | SS | Paracetamol (Unknown) | ACETAMINOPHEN | 1 | Unknown | UNK | U | UNCONFIRMED | 0 | UNK | |||||||
| 125807064 | 12580706 | 11 | SS | PRAVASTATIN. | PRAVASTATIN | 1 | Unknown | 20 MG, DAILY | U | UNCONFIRMED | 0 | 20 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 12 | SS | Salbutamol (Unknown) | ALBUTEROL | 1 | Unknown | 5 MG, DAILY | U | UNCONFIRMED | 0 | 5 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 13 | SS | Tamsulosin (Unknown) | TAMSULOSIN | 1 | Unknown | 400 MG, DAILY | U | UNCONFIRMED | 0 | 400 | MG | UNK | QD | ||||
| 125807064 | 12580706 | 14 | SS | FOSTAIR | BECLOMETHASONEFORMOTEROL | 1 | Unknown | 2 DF, BID | U | 0 | 2 | DF | BID | ||||||
| 125807064 | 12580706 | 15 | SS | LINAGLIPTIN | LINAGLIPTIN | 1 | Unknown | 5 MG, DAILY | U | 0 | 5 | MG | QD | ||||||
| 125807064 | 12580706 | 16 | SS | TAZOCIN | PIPERACILLIN SODIUMTAZOBACTAM SODIUM | 1 | Intravenous (not otherwise specified) | 13.5 G, DAILY | 0 | 13.5 | G | QD | |||||||
| 125807064 | 12580706 | 17 | SS | TAZOCIN | PIPERACILLIN SODIUMTAZOBACTAM SODIUM | 1 | 0 | ||||||||||||
| 125807064 | 12580706 | 18 | SS | TAZOCIN | PIPERACILLIN SODIUMTAZOBACTAM SODIUM | 1 | 0 | ||||||||||||
| 125807064 | 12580706 | 19 | SS | TIOTROPIUM | TIOTROPIUM | 1 | Unknown | 18 ?G, DAILY | U | 0 | 18 | UG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125807064 | 12580706 | 1 | Product used for unknown indication |
| 125807064 | 12580706 | 2 | Product used for unknown indication |
| 125807064 | 12580706 | 3 | Product used for unknown indication |
| 125807064 | 12580706 | 4 | Product used for unknown indication |
| 125807064 | 12580706 | 5 | Product used for unknown indication |
| 125807064 | 12580706 | 6 | Product used for unknown indication |
| 125807064 | 12580706 | 7 | Product used for unknown indication |
| 125807064 | 12580706 | 8 | Product used for unknown indication |
| 125807064 | 12580706 | 9 | Product used for unknown indication |
| 125807064 | 12580706 | 10 | Product used for unknown indication |
| 125807064 | 12580706 | 11 | Product used for unknown indication |
| 125807064 | 12580706 | 12 | Product used for unknown indication |
| 125807064 | 12580706 | 13 | Product used for unknown indication |
| 125807064 | 12580706 | 14 | Product used for unknown indication |
| 125807064 | 12580706 | 15 | Product used for unknown indication |
| 125807064 | 12580706 | 16 | Respiratory failure |
| 125807064 | 12580706 | 17 | Chronic obstructive pulmonary disease |
| 125807064 | 12580706 | 18 | Lower respiratory tract infection |
| 125807064 | 12580706 | 19 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125807064 | 12580706 | DE |
| 125807064 | 12580706 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125807064 | 12580706 | Condition aggravated | |
| 125807064 | 12580706 | Dyspnoea | |
| 125807064 | 12580706 | Oxygen saturation decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |