Egyptian Drug Authority · Egypt
DEA-EG-2026-0061
Tier 1 · Regulator-publishedUnclassifiedتحذير للجمهورStatus · active
- Issuing authority
- Egyptian Drug Authority (EDA)
- Authority reference
- Periodic report no.(61) For 2026
- Date issued
- Jun 2026
- Recorded by us
- 2026-09-06 19:45:29 UTC
- المستحضر
- FLOPADEX 8mg Hard gelatin capsules 30
- INN / active substance
- Not stated by the issuing authority
- Dosage form
- Not stated by the issuing authority
- Strength
- Not stated by the issuing authority
- الشركة المصنعة
- Not stated by the issuing authority
- Manufacturer country
- Not stated by the issuing authority
- MAH or importer
- Not stated by the issuing authority
- أرقام التشغيلات
- 2504626
- تواريخ انتهاء الصلاحية
- Not published with the notice
- Action type
- تحذير للجمهور
- التصنيف
- Not stated by the issuing authority
- Indicative severity
- Not assessed by Drug Eye Africa
- Defect category
- مغشوش
- Product type
- Not stated by the issuing authority
- ATC code
- Not stated by the issuing authority
- Affected markets
- Egypt — no market beyond the issuing country was named on the notice
- Cross-border event
- Not linked to a cross-border event
- نص الإخطار
- FLOPADEX 8mg
Hard gelatin capsules 30
2504626و جميع التشغيلات التي تحمل نفس
الاختلافات الموضحة بالمنشور
رقم التشغيلة
EVA PHARMA
وذلك بناءً على ما ورد الينا من من شركة EVA
PHARMA صاحبة المستحضر حيث افادت ان
العبوات بالاختلافات الموضحة لا تخصها و لم يتم
تصنيعها بمعرفتها.
وقف تداول و ضبط وتحريز المستحضر الغير
مطابق للمواصفات
في حالة الشك في المستحضر الصيدلى يتم الرجوع
الى هيئة الدواء المصرية سواء بالإتصال بالخط
الساخن 15301او الموقع الإلكترونى الخاص
بالهيئة.
يمكن الضغط على الرابطللإطلاع على الصور
الخاصة بالمستحضر المقلد
يونيو 2026
منشور
غش تجاري
اسم المستحضر
الشركة المنتجة
سبب التحذير
الإجراءات
التصحيحية
نصائح
للمستهلكين
هذا التنبيه خاص بالتشغيلات الواردة في المنشور فقط ولا ينطبق على
تداول المستحضر بشكل عامOriginal language: ar
- نص الإخطار بالإنجليزية
- Notice. FLOPADEX 8mg hard gelatin capsules, 30s, of EVA Pharma, batch number 2504626 and every batch showing the same differences described in the circular, on the basis of what EVA Pharma, which owns the product, reported to the Authority.Machine translation, produced by Drug Eye Africa and not checked by the issuing authority. The authority stated only the text above it.
- الحالة
- سارٍ
- Superseded by
- Not superseded. This is the current version.
- Version
- 11
Where this record came from, and what is held to show it.
- Copy of the source
- Taken and held by Drug Eye Africa, so the record survives the link above being moved or withdrawn. Not yet published at an address you can open.Ask us for it and check it against the fingerprint below.
- Fingerprint
- 0e120b884e182ae862a098fc27f5f02ea32192922bef3293ccb938cb3a8bfc80SHA-256 of the copy held. Any file that produces this number is that copy, byte for byte; any file that does not is a different document.
- Copy taken
- 2026-09-06 20:50:27 UTC
| Reference | Date | Country | Product | Batches | Action | Class | Source |
|---|---|---|---|---|---|---|---|
| DEA-XXX-2026-0003 | 03 Jul 2026 | XX | DARZALEX (daratumumab) | MYS7381 · STV1K01 | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0070 | Jul 2026 | EG | Tagrisso 80 mg film-coated tablets | FEST | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-XXX-2026-0002 | 16 Jun 2026 | XX | JAKAVI (ruxolitinib) | none published | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0062 | Jun 2026 | EG | COLOVERIN-D 30 film Coated Tablets | 251035A | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0060 | Jun 2026 | EG | Tears Guard Artificial Tears & Lubricant (Sterile Ophthalmic Solution) | 0425118 | Public warning | Unclassified | Tier 1 · Regulator-published |
Cite this record
Drug Eye Africa (2026). DEA-EG-2026-0061: FLOPADEX 8mg Hard gelatin capsules 30 — تحذير للجمهور, Egyptian Drug Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/eg/2026/dea-eg-2026-0061Version history
v5Manufacturer removed: the named company states the packs are not theirs; the notice describes the packaging as counterfeit (correction)
—Corrections appear here and in the site-wide log. Records are superseded, never deleted.
Verification
Tier 1 — Published by the issuing regulator on its own channel and captured by Drug Eye Africa, with the source document archived.
Indexing
This record is indexable: it is dated, names a product, and carries either a batch number or a stated reason.