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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127622181 | 12762218 | 1 | I | 20160628 | 20160920 | 20160920 | EXP | CZ-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-124244 | RANBAXY | 73.00 | YR | F | Y | 47.00000 | KG | 20160920 | OT | GB | CZ |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127622181 | 12762218 | 1 | SS | Perindopril/Indapamide | INDAPAMIDEPERINDOPRIL | 1 | Unknown | UNK | Y | 0 | |||||||||
127622181 | 12762218 | 2 | PS | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | Unknown | 150 MG, DAILY | U | 73137 | 150 | MG | |||||||
127622181 | 12762218 | 3 | SS | Amiloride, Hydrochlorothiazide | AMILORIDE HYDROCHLORIDEHYDROCHLOROTHIAZIDE | 1 | Unknown | Y | 0 | ||||||||||
127622181 | 12762218 | 4 | C | Lacidipine | LACIDIPINE | 1 | Unknown | 4 MG IN THE MORNING AND 2 MG IN THE EVENING | U | 0 | |||||||||
127622181 | 12762218 | 5 | C | Acebutolol | ACEBUTOLOL | 1 | Unknown | 400 MG, BID | U | 0 | 400 | MG | Q12H | ||||||
127622181 | 12762218 | 6 | C | Acetylsalicylic acid | ASPIRIN | 1 | Unknown | 100 MG, DAILY | U | 0 | 100 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127622181 | 12762218 | 1 | Hypertension |
127622181 | 12762218 | 2 | Depression |
127622181 | 12762218 | 3 | Hypertension |
127622181 | 12762218 | 4 | Product used for unknown indication |
127622181 | 12762218 | 5 | Product used for unknown indication |
127622181 | 12762218 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127622181 | 12762218 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127622181 | 12762218 | Hyponatraemia | |
127622181 | 12762218 | Multiple fractures | |
127622181 | 12762218 | Osteoporosis |
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 |
---|---|---|---|---|---|---|
127622181 | 12762218 | 3 | 2006 | 0 |