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Scientific & Prescribing Resources

HonniHil® information for healthcare professionals

Professional product, prescribing, safety and medical-information resources relating to HonniHil® tadalafil 20 mg tablets.

This page provides a structured professional overview. The current locally approved prescribing information remains the controlling source for indication, dosage, contraindications, warnings and adverse reactions.

HonniHil tadalafil 20 mg pack and four-tablet blister
Confirm that the displayed pack matches the current approved market presentation.

Product at a glance

Core HonniHil® product information

These details should be checked against the current approved pack, product dossier and NAFDAC documentation before publication.

Brand HonniHil®
Active ingredient Tadalafil
Strength 20 mg
Dosage form Film-coated tablets
Presentation 1 × 4 tablets
Therapeutic class PDE5 inhibitor
Legal status Prescription medicine
NAFDAC registration B4-1293
Manufacturer Fredun Pharmaceuticals Ltd.
Product company Lyn-Edge Pharmaceuticals Ltd.

Approved indication

Management of erectile dysfunction

HonniHil® contains tadalafil and is intended for use in adult men with erectile dysfunction under the direction of a qualified prescriber.

Regulatory control: Use the exact indication wording in the current NAFDAC-approved prescribing information. Do not extend the indication to premature ejaculation, relationship outcomes or unapproved patient groups.

Mechanism summary

Tadalafil selectively inhibits phosphodiesterase type 5. During sexual stimulation, PDE5 inhibition increases cGMP-mediated smooth muscle relaxation and supports increased penile blood flow.

View the full mechanism page →
Medical infographic showing the nitric oxide cGMP and PDE5 pathway for tadalafil
Simplified educational graphic. Use approved technical materials for formal scientific or promotional communication.

Prescribing overview

Use the current approved prescribing information

Dosage and administration may depend on indication, renal or hepatic function, concomitant medicines and individual tolerability. The website should not replace the approved local prescribing document.

Dosage and administration

Display the exact authorised dose, timing, maximum frequency and food instructions from the current HonniHil® prescribing information.

Renal and hepatic impairment

Confirm whether dose adjustment, reduced frequency or avoidance is required for specific degrees of renal or hepatic impairment.

Special populations

Use approved recommendations for older adults, patients with cardiovascular disease and populations not included in the indication.

Concomitant therapy

Review alpha blockers, antihypertensives, CYP3A4 inhibitors or inducers and other erectile-dysfunction treatments before prescribing.

Do not publish dosing from a generic tadalafil label

The dose shown on the HonniHil® pack does not by itself define the complete dosing instruction. Use the current locally approved document.

Open Prescribing Information

Contraindications and precautions

Key safety areas for professional review

This is a high-level summary only. Refer to the approved SmPC or prescribing information for complete wording and clinical decision-making.

01

Organic nitrates

Tadalafil is contraindicated with organic nitrates because it can potentiate their hypotensive effect.

02

Guanylate cyclase stimulators

Concomitant use with medicines such as riociguat may increase hypotensive effects and is contraindicated in reference labels.

03

Cardiovascular status

Assess whether sexual activity and PDE5-inhibitor treatment are appropriate for the patient’s cardiovascular condition.

04

Hypotension

Consider additive blood-pressure effects with alpha blockers, antihypertensives and substantial alcohol intake.

05

Priapism and penile conditions

Use caution in patients predisposed to prolonged erection or with anatomical penile conditions.

06

Vision and hearing events

Counsel patients on urgent assessment for sudden vision or hearing changes.

07

Renal and hepatic function

Apply the approved dose limitations and monitoring recommendations.

08

Hypersensitivity

Do not prescribe to patients with serious hypersensitivity to tadalafil or another ingredient.

Clinically relevant interactions

Review the complete medicine list

Consider prescription medicines, non-prescription products, supplements, alcohol and recreational substances.

Medicine or factor
Professional consideration
Organic nitrates
Contraindicated because of potentially severe hypotension.
Riociguat or other GC stimulators
Contraindicated in reference tadalafil labels.
Alpha blockers
Potential additive hypotension; review stability, dose and timing.
Antihypertensives
Monitor for additive blood-pressure reduction where clinically appropriate.
Potent CYP3A4 inhibitors
May increase tadalafil exposure; apply the approved dosing limitation.
CYP3A4 inducers
May reduce tadalafil exposure and therapeutic response.
Other PDE5 inhibitors or ED treatments
Combination safety and efficacy are not established; avoid unapproved combination use.
Substantial alcohol intake
May increase orthostatic symptoms, dizziness or hypotension.

Adverse reactions

Use approved frequency categories

Tadalafil reference labels commonly describe headache, dyspepsia, back pain, myalgia, nasal congestion, flushing and pain in the limbs.

Do not publish a frequency table until the categories and percentages have been checked against the current HonniHil® prescribing information.

Events requiring urgent assessment or discontinuation advice

  • Priapism or an erection lasting longer than four hours.
  • Sudden vision loss or significant visual change.
  • Sudden hearing loss or severe auditory symptoms.
  • Severe hypersensitivity reaction.
  • Chest pain, syncope or serious cardiovascular symptoms.
Healthcare professional discussing a clinical question during a consultation

Medical and safety support

Direct professional enquiries to the right team

Separate medical-information requests, adverse-event reports and product-quality complaints. They require different review and follow-up processes.

Professional information notice: This page is a structured website draft and does not replace the current NAFDAC-approved prescribing information, SmPC, product dossier or clinical judgement.

Reference sources used for the draft
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