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cer
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0.23
entities
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0.04
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audioduration (s)
5.01
16.1
Please evaluate Mr. Jones for eligibility for depemokimab, as he has severe eosinophilic asthma despite current therapy.
Please evaluate Mr. Jones for eligibility for Dipemicimab, as he has severe eosinophilic asthma despite current therapy.
0.058824
0.025641
"[{\"text\": \"depemokimab\", \"category\": \"drug\", \"char_start\": 46, \"char_end\": 57}]"
0.363636
Abdominal ultrasound performed to assess liver parenchyma given patient's history of familial chylomicronemia syndrome and initiation of plozasiran.
Abdominal ultrasound, performed to assess liver parenchyma, given patients history of familial chylomicronemia syndrome and initiation of plazoscerin.
0.111111
0.040816
"[{\"text\": \"plozasiran\", \"category\": \"drug\", \"char_start\": 137, \"char_end\": 147}]"
0.4
Patients receiving donidalorsen demonstrated a significant reduction in the frequency of hereditary angioedema attacks during the study period.
Patients receiving Donadellerson demonstrated a significant reduction in the frequency of hereditary angiotoma attacks during the study period.
0.111111
0.056338
"[{\"text\": \"donidalorsen\", \"category\": \"drug\", \"char_start\": 19, \"char_end\": 31}]"
0.416667
Patient discharged with a prescription for tradipitant for motion sickness prevention.
Patient discharged with a prescription for tradipident for motion sickness prevention.
0.090909
0.023529
"[{\"text\": \"tradipitant\", \"category\": \"drug\", \"char_start\": 43, \"char_end\": 54}]"
0.181818
Initiate gepotidacin 1500 mg BID for three days for her acute uncomplicated cystitis.
initiate Jepatiticin fifteen hundred MG bid for three days for her acute, uncomplicated cystitis.
0.230769
0.22619
"[{\"text\": \"gepotidacin\", \"category\": \"drug\", \"char_start\": 9, \"char_end\": 20}]"
0.363636
Prescribe fitusiran, 80 mg subcutaneously once monthly, for bleeding prophylaxis in this patient with hemophilia B and inhibitors.
Prescribe fiducerin, ADMG subcutaneously once monthly, for bleeding prophylaxis in this patient with hemophilia B and inhibitors.
0.166667
0.055118
"[{\"text\": \"fitusiran\", \"category\": \"drug\", \"char_start\": 10, \"char_end\": 19}]"
0.444444
Given his persistent symptoms from obstructive hypertrophic cardiomyopathy, we are referring him for a cardiology opinion regarding aficamten.
Given his persistent symptoms from obstructive hypertrophic cardiomyopathy, we are referring him for a cardiology opinion regarding a ficampton.
0.111111
0.021429
"[{\"text\": \"aficamten\", \"category\": \"drug\", \"char_start\": 132, \"char_end\": 141}]"
0.111111
Clinical history includes familial chylomicronemia syndrome, currently managed with olezarsen, presenting with epigastric discomfort.
Clinical history includes familial chilomicronemia syndrome, currently managed with Olzarson, presenting with epigastric discomfort.
0.142857
0.023077
"[{\"text\": \"olezarsen\", \"category\": \"drug\", \"char_start\": 84, \"char_end\": 93}]"
0.333333
Initiate levacetylleucine for the neurological manifestations of Niemann-Pick type C disease.
Initiate levocetoleucne for the neurological manifestations of Nemanpic Type C disease.
0.25
0.086957
"[{\"text\": \"levacetylleucine\", \"category\": \"drug\", \"char_start\": 9, \"char_end\": 25}]"
0.25
Plan to initiate therapy with obecabtagene autoleucel for the patient's relapsed B-cell acute lymphoblastic leukemia.
Plan to initiate therapy with Obecoptagen autolucal for the patient's relapsed B cell, acute lymphoblastic leukemia.
0.125
0.043103
"[{\"text\": \"obecabtagene autoleucel\", \"category\": \"drug\", \"char_start\": 30, \"char_end\": 53}]"
0.26087
The patient was randomized to receive inavolisib in combination with palbociclib and fulvestrant as per the study arm.
The patient was randomized to receive enavelisb in combination with palbiclib and full vestrant, as per the study arm.
0.222222
0.059829
"[{\"text\": \"inavolisib\", \"category\": \"drug\", \"char_start\": 38, \"char_end\": 48}]"
0.3
We plan to initiate sibeprenlimab for her IgA nephropathy to help reduce her significant proteinuria.
We plan to initiate Cyprin Limab for her Ig A nephropathy to help reduce her significant protonuria.
0.333333
0.09
"[{\"text\": \"sibeprenlimab\", \"category\": \"drug\", \"char_start\": 20, \"char_end\": 33}]"
0.461538
Topical beremagene geperpavec was discussed with the family as a potential treatment option for the patient's dystrophic epidermolysis bullosa wounds.
Topical Berimaging Jepopavic was discussed with the family as a potential treatment option for the patient's dystrophic epidermolysis bullosa wounds.
0.1
0.04698
"[{\"text\": \"beremagene geperpavec\", \"category\": \"drug\", \"char_start\": 8, \"char_end\": 29}]"
0.380952
Overall, the extent of metastatic disease remains stable on current zongertinib therapy.
Overall, the extent of metastatic disease remains stable on current zongotinib therapy.
0.083333
0.023256
"[{\"text\": \"zongertinib\", \"category\": \"drug\", \"char_start\": 68, \"char_end\": 79}]"
0.181818
Following surgical resection, we are initiating vorasidenib as adjuvant therapy for his IDH-mutant grade 2 astrocytoma.
Following surgical resection, we are initiating Voricidnib as adjuvant therapy for his IDH mutant grade 2 astrocytoma.
0.058824
0.025641
"[{\"text\": \"vorasidenib\", \"category\": \"drug\", \"char_start\": 48, \"char_end\": 59}]"
0.363636
Prescribe paltusotine 30 mg orally once daily for ongoing management of her acromegaly.
Prescribe poltusatine 30 mg orally once daily for ongoing management of her acromegaly.
0.076923
0.023256
"[{\"text\": \"paltusotine\", \"category\": \"drug\", \"char_start\": 10, \"char_end\": 21}]"
0.181818
Brain MRI demonstrates no acute intracranial pathology to account for the patient's menopausal vasomotor symptoms, currently managed with elinzanetant.
Brain MRI demonstrates no acute intracranial pathology to account for the patient's menopausal vasomotor symptoms, currently managed with a linzenetant.
0.105263
0.020134
"[{\"text\": \"elinzanetant\", \"category\": \"drug\", \"char_start\": 138, \"char_end\": 150}]"
0.166667
Given the recent FDA approval, we plan to initiate the patient on doxecitine and doxribtimine for their thymidine kinase 2 deficiency.
Given the recent FDA approval, we plan to initiate the patient on darksicetine and darksriptamine for their thymidine kinase 2 deficiency.
0.095238
0.090909
"[{\"text\": \"doxecitine and doxribtimine\", \"category\": \"drug\", \"char_start\": 66, \"char_end\": 93}]"
0.296296
The patient received a single oral dose of zoliflodacin for the treatment of uncomplicated urogenital gonorrhea.
the patient received a single oral dose of xaliflarticin for the treatment of uncomplicated urogenital gonorrhea.
0.0625
0.054054
"[{\"text\": \"zoliflodacin\", \"category\": \"drug\", \"char_start\": 43, \"char_end\": 55}]"
0.416667
Considering his persistently elevated LDL despite maximal statin therapy, we are evaluating the potential for initiating lerodalcibep as a monthly subcutaneous option.
Considering his persistently elevated LDL despite maximal statin therapy, we are evaluating the potential for initiating Leridalcybup as a monthly subcutaneous option.
0.045455
0.018182
"[{\"text\": \"lerodalcibep\", \"category\": \"drug\", \"char_start\": 121, \"char_end\": 133}]"
0.333333
Datopotamab deruxtecan demonstrated a statistically significant improvement in progression-free survival compared to standard of care in the study population.
Datapotomab Derek Stecken demonstrated a statistically significant improvement in progression-free survival compared to standard of care in the study population.
0.15
0.050955
"[{\"text\": \"Datopotamab deruxtecan\", \"category\": \"drug\", \"char_start\": 0, \"char_end\": 22}]"
0.272727
Patient discharged on nerandomilast 25 mg twice daily for continued management of her idiopathic pulmonary fibrosis.
Patient discharged on Narendomolast twenty five MG twice daily for continued management of her idiopathic pulmonary fibrosis.
0.1875
0.121739
"[{\"text\": \"nerandomilast\", \"category\": \"drug\", \"char_start\": 22, \"char_end\": 35}]"
0.307692
The patient was discharged on resmetirom for their noncirrhotic MASH with moderate liver fibrosis, per recent EMA approval.
The patient was discharged on Rasmedirom for their non-cerrhotic mash with moderate liver fibrosis, per recent EMA approval.
0.166667
0.033058
"[{\"text\": \"resmetirom\", \"category\": \"drug\", \"char_start\": 30, \"char_end\": 40}]"
0.3
Start penpulimab 200 mg IV every three weeks for recurrent nasopharyngeal carcinoma.
Start Pempulumab 200 Mg every three weeks for recurrent nasopharyngeal carcinoma.
0.166667
0.060241
"[{\"text\": \"penpulimab\", \"category\": \"drug\", \"char_start\": 6, \"char_end\": 16}]"
0.3
Initiate ziftomenib 200 mg orally once daily for relapsed NPM1-mutated AML, monitoring for differentiation syndrome.
Initiate ZYFTOMIB 200 Mg orally once daily, for relapsed NPM1 mutated AML, monitoring for differentiation syndrome.
0.0625
0.026316
"[{\"text\": \"ziftomenib\", \"category\": \"drug\", \"char_start\": 9, \"char_end\": 19}]"
1
No acute changes demonstrated on orbital CT; patient continues acoltremon for chronic dry eye disease.
No acute changes demonstrated on orbital CT. Patient continues aclumin for chronic dry eye disease.
0.066667
0.05
"[{\"text\": \"acoltremon\", \"category\": \"drug\", \"char_start\": 63, \"char_end\": 73}]"
0.5
Clinical history notes IgA nephropathy with significant proteinuria, for which the patient recently initiated atrasentan.
Clinical History notes Ig A nephropathy with significant protonuria, for which the patient recently initiated at Racinton.
0.333333
0.058824
"[{\"text\": \"atrasentan\", \"category\": \"drug\", \"char_start\": 110, \"char_end\": 120}]"
0.4
Follow-up MRI of the lower extremities performed to assess disease progression in a Duchenne patient receiving givinostat.
Follow-up MRI of the lower extremities performed to assess disease progression in a Duchenne patient receiving givenastat.
0.055556
0.016529
"[{\"text\": \"givinostat\", \"category\": \"drug\", \"char_start\": 111, \"char_end\": 121}]"
0.2
We are referring Mr. Smith for consideration of telisotuzumab vedotin given his locally advanced non-squamous NSCLC with high c-Met overexpression.
We are referring Mr. Smith for consideration of Telesatu Zumubveditin, given his locally advanced non squamous NSCLC, with high CMET overexpression.
0.181818
0.048276
"[{\"text\": \"telisotuzumab vedotin\", \"category\": \"drug\", \"char_start\": 48, \"char_end\": 69}]"
0.333333
We are considering garadacimab for prophylaxis to prevent further hereditary angioedema attacks in this patient.
We are considering Gyaradasimab for prophylaxis to prevent further hereditary angiodoma attacks in this patient.
0.133333
0.036036
"[{\"text\": \"garadacimab\", \"category\": \"drug\", \"char_start\": 19, \"char_end\": 30}]"
0.181818
We are considering initiating narsoplimab for her refractory transplant-associated thrombotic microangiopathy.
We are considering initiating Narciplema for her refractory, transplant-associated thrombotic microangiopathy.
0.083333
0.036697
"[{\"text\": \"narsoplimab\", \"category\": \"drug\", \"char_start\": 30, \"char_end\": 41}]"
0.454545
Patient discharged with a prescription for suzetrigine 50 mg twice daily for ongoing acute pain management.
Patient discharged with a prescription for Suzitrogen 50 Mg twice daily for ongoing acute pain management.
0.0625
0.037736
"[{\"text\": \"suzetrigine\", \"category\": \"drug\", \"char_start\": 43, \"char_end\": 54}]"
0.454545
Prescribe sebetralstat 80 mg by mouth as needed for acute hereditary angioedema attacks.
Prescribe Sebatralstat AD Mg by mouth as needed for acute hereditary angiodoma attacks.
0.230769
0.057471
"[{\"text\": \"sebetralstat\", \"category\": \"drug\", \"char_start\": 10, \"char_end\": 22}]"
0.166667
Patient was started on delgocitinib cream for her moderate-to-severe chronic hand eczema due to inadequate response to previous topical treatments.
Patient was started on delgacitonib cream for her moderate to severe chronic hand eczema, due to inadequate response to previous topical treatments.
0.045455
0.013699
"[{\"text\": \"delgocitinib\", \"category\": \"drug\", \"char_start\": 23, \"char_end\": 35}]"
0.166667
Patients receiving dordaviprone demonstrated a statistically significant improvement in overall survival compared to placebo.
Patients receiving Dordoviprone demonstrated a statistically significant improvement in overall survival compared to placebo.
0.071429
0.008065
"[{\"text\": \"dordaviprone\", \"category\": \"drug\", \"char_start\": 19, \"char_end\": 31}]"
0.166667
Stable disease noted in the setting of ongoing avutometinib therapy.
stable disease noted in the setting of ongoing avutometanip therapy.
0.1
0.029851
"[{\"text\": \"avutometinib\", \"category\": \"drug\", \"char_start\": 47, \"char_end\": 59}]"
0.166667
Patients in cohort A received a single infusion of etuvetidigene autotemcel following myeloablative conditioning.
Patients in cohort A received a single infusion of etuvetidygene autotempsil following myeloablative conditioning.
0.142857
0.035714
"[{\"text\": \"etuvetidigene autotemcel\", \"category\": \"drug\", \"char_start\": 51, \"char_end\": 75}]"
0.125
No acute intracranial hemorrhage or significant lymphadenopathy is identified in this patient with Wiskott-Aldrich syndrome.
No acute intracranial hemorrhage or significant lymphatinopathy is identified in this patient with Wisko-Taldrich syndrome.
0.1875
0.03252
"[{\"text\": \"Wiskott-Aldrich syndrome\", \"category\": \"condition\", \"char_start\": 99, \"char_end\": 123}]"
0.166667
We are referring this patient for allogeneic hematopoietic stem cell transplantation, and recommend a preparative conditioning regimen including treosulfan.
We are referring this patient for allogeneic hematopoietic stem cell transplantation, and recommend a preparative conditioning regimen, including triosulfin.
0.052632
0.012987
"[{\"text\": \"treosulfan\", \"category\": \"drug\", \"char_start\": 145, \"char_end\": 155}]"
0.2
We are evaluating aceclidine as a potential non-surgical treatment for her symptomatic presbyopia to enhance near vision.
We are evaluating a seclidine as a potential non-surgical treatment for her symptomatic presbyopia to enhance near vision.
0.111111
0.016667
"[{\"text\": \"aceclidine\", \"category\": \"drug\", \"char_start\": 18, \"char_end\": 28}]"
0.1
Plan for Meduloc intramedullary fixation of the right fifth metacarpal shaft fracture.
Plan for medularc intramedullary fixation of the right fifth metacarpal shaft fracture.
0.083333
0.023529
"[{\"text\": \"Meduloc intramedullary fixation\", \"category\": \"procedure\", \"char_start\": 9, \"char_end\": 40}]"
0.064516
Given the diagnosis of H3 K27M-mutant diffuse midline glioma, please prescribe dordaviprone as per protocol.
Given the diagnosis of H three K twenty seven M mutant diffuse midline glioma, please prescribe Dordovipron as per protocol.
0.4375
0.207547
"[{\"text\": \"H3 K27M-mutant diffuse midline glioma\", \"category\": \"condition\", \"char_start\": 23, \"char_end\": 60}]"
0.108108
No new intracranial abnormalities are identified following the initiation of sepiapterin.
No new intracranial abnormalities are identified following the initiation of Sepiapterin.
0
0
"[{\"text\": \"sepiapterin\", \"category\": \"drug\", \"char_start\": 77, \"char_end\": 88}]"
0.090909
Initiate pembrolizumab and berahyaluronidase alfa subcutaneously for her metastatic lung adenocarcinoma.
Initiate pembrolizumab and barrachialeronidase, alpha subcutaneously for her metastatic lung adenocarcinoma.
0.181818
0.067961
"[{\"text\": \"pembrolizumab and berahyaluronidase alfa\", \"category\": \"drug\", \"char_start\": 9, \"char_end\": 49}]"
0.1
Eligible subjects with inoperable plexiform neurofibromas due to neurofibromatosis type 1 were randomized to mirdametinib or placebo.
Eligible subjects with inoperable plexiform neurofibromas, due to neurofibromatosis Type I were randomized to mydometanib or placebo.
0.117647
0.037879
"[{\"text\": \"mirdametinib\", \"category\": \"drug\", \"char_start\": 109, \"char_end\": 121}]"
0.333333
Eligibility for dordaviprone required confirmation of the H3 K27M histone mutation in patients with diffuse midline glioma.
Eligibility for Dordoviprone required confirmation of the H3K 27M histone mutation in patients with diffuse midline glioma.
0.176471
0.02459
"[{\"text\": \"H3 K27M histone mutation\", \"category\": \"biomarker\", \"char_start\": 58, \"char_end\": 82}]"
0.041667
Patient will be discharged on oral elamipretide 40 mg twice daily for his Barth syndrome, with close follow-up.
Patient will be discharged on oral alamopredide 40 Mg twice daily for his Barth syndrome, with close follow-up.
0.052632
0.027523
"[{\"text\": \"elamipretide\", \"category\": \"drug\", \"char_start\": 35, \"char_end\": 47}]"
0.25
Start sevabertinib 150 mg PO BID for HER2-mutated NSCLC with CNS metastases.
Start Sevabertin at 150 MG Po bid for HER two mutated NSCLC with CNS metastases.
0.307692
0.093333
"[{\"text\": \"sevabertinib\", \"category\": \"drug\", \"char_start\": 6, \"char_end\": 18}]"
0.25
Follow-up CT scan demonstrates stable osseous disease, indicating a persistent response to linvoseltamab treatment.
Follow-up CT scan demonstrates stable osseous disease, indicating a persistent response to linvosaltamab treatment.
0.066667
0.00885
"[{\"text\": \"linvoseltamab\", \"category\": \"drug\", \"char_start\": 91, \"char_end\": 104}]"
0.076923
The patient is discharged home to continue sunvozertinib 300 mg daily for their EGFR exon 20 insertion mutated NSCLC.
The patient is discharged home to continue Sunvosertinib three hundred MG daily for their EGFR Exxon twenty insertion, mutated NSCLC.
0.263158
0.181034
"[{\"text\": \"sunvozertinib\", \"category\": \"drug\", \"char_start\": 43, \"char_end\": 56}]"
0.153846

Evaluation Results: parakeet-tdt-0.6b-v3

Evaluation results from Whisper model evaluation.

Summary

Model WER CER
nvidia/parakeet-tdt-0.6b-v3 11.34% 3.63%

Source Data

Columns

Column Description
audio Audio sample (if available from source dataset)
reference Ground truth transcription
prediction Model prediction
wer Word Error Rate for this sample
cer Character Error Rate for this sample

| entities | Entity annotations from source dataset | | entity_cer | Per-sample entity CER (-1.0 if no entities) |

Entity CER

Overall Entity CER: 24.62%

Category CER
biomarker 4.17%
condition 13.11%
drug 27.48%
procedure 6.45%

Generated by Trelis Studio

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