Terazosin

Evidence Level: L5 Predicted Indications: 10

Table of Contents

  1. Terazosin
    1. Pharmacist Assessment Report
    2. Terazosin: Hypotrichosis simplex of the scalp
    3. One-Sentence Summary
    4. Quick Overview
    5. Why is This Prediction Reasonable?
      1. Other Predicted Indications (Top 10)
    6. Clinical Trial Evidence
    7. Literature Evidence
    8. Canada Market Information
    9. Safety Considerations
    10. Conclusion and Next Steps
    11. Disclaimer

Pharmacist Assessment Report

Terazosin: Hypotrichosis simplex of the scalp

One-Sentence Summary

Terazosin is an alpha-1 adrenergic blocker originally used to treat hypertension and benign prostatic hyperplasia (BPH). The TxGNN model’s top-ranked prediction is hypotrichosis simplex of the scalp, but there are no clinical trials and no publications supporting it, so this is a model-only prediction. Among the other predicted indications, Raynaud disease (1 publication) and migraine (2 publications) have the most supporting evidence.


Quick Overview

Item Content
Original Indication Not recorded in the local data
Predicted New Indication Hypotrichosis simplex of the scalp
TxGNN Prediction Score 0.9997
Evidence Level L5
Canada Market Status Marketed (marketed DINs: 8 of 8)
Number of DINs 8 (marketed: 8)
Recommended Decision Hold

Why is This Prediction Reasonable?

Currently, detailed mechanism of action data is not available from the compiled data. Based on known pharmacology, terazosin is an alpha-1 adrenergic antagonist that relaxes vascular and prostatic smooth muscle. This explains its efficacy in hypertension and BPH.

For the top prediction, hypotrichosis simplex of the scalp (score 0.9997), the link is speculative. One could argue that vasodilation might improve hair follicle perfusion, similar to minoxidil. However, hypotrichosis simplex is a genetic disorder, so a vasodilator is unlikely to address its root cause. The high score comes from the TxGNN model (deep learning) and may reflect similarities the model learned between related diseases, such as other hair-related conditions, not biological evidence.

The more plausible candidates are those tied to adrenergic vasoregulation. Raynaud disease has the strongest rationale: cold-induced vasospasm is driven by adrenergic vasoconstriction, and alpha-1 blockade produces peripheral vasodilation. Migraine is a second, weaker candidate, based on possible effects on adrenergic tone and cerebrovascular reactivity.

Other Predicted Indications (Top 10)

Rank Predicted Indication Score Evidence Level Recommendation
1 Hypotrichosis simplex of the scalp 0.9997 L5 Hold
2 Congenital hypotrichosis milia 0.9997 L5 Hold
3 Diffuse alopecia areata 0.9996 L5 Hold
4 Alopecia 0.9995 L5 Hold
5 Migraine disorder 0.9992 L4 Research Question
6 Migraine with brainstem aura 0.9991 L5 Hold
7 Raynaud disease 0.9983 L3 Research Question
8 Ambras type hypertrichosis universalis congenita 0.9965 L5 Hold
9 Manic bipolar affective disorder 0.9955 L5 Hold
10 Kyphoscoliotic heart disease 0.9949 L5 Hold

Clinical Trial Evidence

Currently no related clinical trials are registered for the top-ranked prediction (hypotrichosis simplex of the scalp). No trials were found for any of the other nine predicted indications either.


Literature Evidence

No literature is available for the top-ranked prediction. The table below lists the publications found for lower-ranked predictions, which are the only supporting literature in the compiled data.

PMID Year Type Journal Related Indication Key Findings
9273472 1997 Clinical study (design unverified) Minerva Cardioangiologica Raynaud disease Terazosin reduced the number, intensity and duration of vasospastic attacks in idiopathic and secondary Raynaud’s phenomenon, with improved thermographic and ultrasonographic findings.
7911406 1994 Clinical study (small, open trial) La Clinica Terapeutica Migraine Open trial in 46 patients with migraine without aura comparing terazosin (10 patients), buflomedil (29) and both (7) for prophylaxis.
9074296 1997 Review / case series Headache Migraine Ten patients given terazosin or doxazosin; all but one had reduced migraine frequency or severity, but 5 stopped because of side effects.
34779371 2022 Review Current Cardiology Reviews Alopecia Review of non-cardiac effects of cardiovascular drugs, including hair effects of vasoactive agents such as minoxidil. It does not show terazosin efficacy in alopecia.

Canada Market Information

DIN Product Name Dosage Form Approved Indication
02243521 PMS-TERAZOSIN Not specified Not specified
02234503 APO-TERAZOSIN Not specified Not specified
02243519 PMS-TERAZOSIN Not specified Not specified
02243518 PMS-TERAZOSIN Not specified Not specified
02243520 PMS-TERAZOSIN Not specified Not specified

Eight valid single-ingredient licences are held in total (PMS-TERAZOSIN and APO-TERAZOSIN); the five above are shown.


Safety Considerations

  • Contraindication-related conditions (from the knowledge graph, not label text): multiple system atrophy, postural orthostatic tachycardia syndrome, orthostatic hypotension, priapism, intraoperative floppy iris syndrome.
  • Drug Interactions: 100 interactions were identified. The ones listed are mostly of Moderate severity and include:
    • Corticosteroids: hydrocortisone, prednisone, prednisolone, dexamethasone, betamethasone, budesonide, triamcinolone
    • Opioids: morphine (including liposomal), opium
    • SGLT2 inhibitors: canagliflozin, dapagliflozin, empagliflozin, ertugliflozin
    • Cannabinoids: dronabinol, nabilone
    • Others: bupropion
    • Unknown severity: calcitriol, pantoprazole, glimepiride
  • Practical concern: for Raynaud disease, hypotension, dizziness and first-dose syncope are the main concerns, particularly in patients who already have low blood pressure.

Please refer to the package insert for the full warnings and contraindications.


Conclusion and Next Steps

Decision: Hold

Rationale: The top-ranked prediction, hypotrichosis simplex of the scalp, has a very high model score but no trials, no literature, and an implausible mechanism for a genetic disorder. The evidence is Level L5. Of the lower-ranked predictions, Raynaud disease (L3) and migraine (L4) merit follow-up as research questions, but the supporting studies are old, small and of unverified design.

To proceed, the following is needed:

  • Package insert warnings and contraindications from Health Canada (a blocking gap for safety screening)
  • Detailed mechanism of action data from DrugBank
  • For Raynaud disease: the full text of PMID 9273472 to confirm design, sample size and outcomes, followed by a search for modern controlled trials
  • For migraine: a review of whether newer controlled data exist for alpha-1 blockers in prophylaxis
  • A blood pressure monitoring and first-dose safety plan for any trial in populations prone to low blood pressure

    Disclaimer

This content is for research purposes only and does not constitute medical advice. Clinical validation is required before any clinical application.



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