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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 110879754 | 11087975 | 4 | F | 20150130 | 20160727 | 20150504 | 20160803 | EXP | PHHY2014AU131231 | NOVARTIS | 57.40 | YR | F | Y | 0.00000 | 20160803 | MD | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 110879754 | 11087975 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 20 MG | U | SO207 | 21008 | 20 | MG | ||||||
| 110879754 | 11087975 | 2 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | U | 0 | ||||||||||
| 110879754 | 11087975 | 3 | C | KARVEA | IRBESARTAN | 1 | Oral | 75 MG, DAILY | U | 0 | 75 | MG | TABLET | QD | |||||
| 110879754 | 11087975 | 4 | C | NORMISON | TEMAZEPAM | 1 | Oral | 10 MG, 1 TO 3, NOCTE, P.R.N. | U | 0 | 10 | MG | |||||||
| 110879754 | 11087975 | 5 | C | NATRILIX - SLOW RELEASE | INDAPAMIDE | 1 | Oral | 1.5 MG, DAILY | U | 0 | 1.5 | MG | QD | ||||||
| 110879754 | 11087975 | 6 | C | ONDANSETRON | ONDANSETRON | 1 | Oral | 8 MG, 1 TABLET, PRN | U | 0 | 8 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 110879754 | 11087975 | 1 | Acromegaly |
| 110879754 | 11087975 | 2 | Acromegaly |
| 110879754 | 11087975 | 3 | Hypertension |
| 110879754 | 11087975 | 4 | Insomnia |
| 110879754 | 11087975 | 5 | Hypertension |
| 110879754 | 11087975 | 6 | Vomiting |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 110879754 | 11087975 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 110879754 | 11087975 | Abdominal pain | |
| 110879754 | 11087975 | Abdominal pain upper | |
| 110879754 | 11087975 | Anxiety | |
| 110879754 | 11087975 | Back pain | |
| 110879754 | 11087975 | Blood pressure increased | |
| 110879754 | 11087975 | Cholelithiasis | |
| 110879754 | 11087975 | Drug ineffective | |
| 110879754 | 11087975 | Dyspepsia | |
| 110879754 | 11087975 | Feeling abnormal | |
| 110879754 | 11087975 | Gastrooesophageal reflux disease | |
| 110879754 | 11087975 | Hyperthyroidism | |
| 110879754 | 11087975 | Insomnia | |
| 110879754 | 11087975 | Malaise | |
| 110879754 | 11087975 | Mood swings | |
| 110879754 | 11087975 | Needle issue | |
| 110879754 | 11087975 | Pain in extremity | |
| 110879754 | 11087975 | Sleep disorder | |
| 110879754 | 11087975 | Vertigo |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |