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Cerebrolysin
Cerebrolysin
Cerebrolysin
Cerebrolysin 60mg
Cerebrolysin 60mg
Cerebrolysin 60mg
Cerebrolysin 60mg
Cerebrolysin 60mg
Compare 13 prices for Cerebrolysin. Cheapest: £17.95. Average: £38.79.
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| £41.00 | £0.68/mg | In Stock | Free over £100 |
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| £17.95 | £0.30/mg | Out of Stock | Free over £75 |
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| £34.99 | £0.58/mg | In Stock | Free |
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| £19.95 | £0.33/mg | Out of Stock | Free |
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| £75.00 | £1.25/mg | In Stock | Free |
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| £33.00 | £0.55/mg | In Stock | Free |
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| £24.99 | £0.42/mg | In Stock | Free |
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| £25.00 £22.50 | £0.38/mg | In Stock | Free |
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| £24.90 | £0.42/mg | In Stock | Free |
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| £25.00 | £0.42/mg | In Stock | Free |
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| £25.00 | £0.42/mg | In Stock | Free over £200 |
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| £30.00 | £0.50/mg | Out of Stock | £9.99 |
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| £130.00 | £2.17/mg | In Stock | Free |
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Neuropeptide Preparation | Neurological Recovery
Standardized neuropeptide preparation containing bioactive peptides and amino acids exhibiting neurotrophic and neuroprotective properties for stroke recovery, traumatic brain injury, and cognitive enhancement. Used clinically in 50+ countries.
IV/IM administration provides optimal bioavailability and brain penetration of neuropeptides and neurotrophic factors.
Bioactive peptide mixture
Meta-analyses show modest cognitive improvements, though clinical significance remains debated.
Multiple RCTs demonstrate significant ADAS-cog and CIBIC+ improvements.
Large meta-analysis shows significant NIHSS improvements; other studies found no functional benefit.
Largest meta-analysis (1,879 patients) shows NIHSS benefits; independent analysis found no mRS improvement.
Multiple trials including CAPTAIN series confirm GCS/GOS improvements.
Pilot trial shows promising 6-month outcomes; requires larger confirmatory studies.
Some studies show enhanced recovery; results vary significantly between trials.
Early administration within 72 hours shows better outcomes than delayed treatment.
Primary administration route with well-established protocols for direct brain delivery via IV/IM.
| Goal | Dose | Frequency | Route |
|---|---|---|---|
| Small Volume IV | Up to 10mL | Once daily | Undiluted IV slow push over 3 minutes |
| Intramuscular | Up to 5mL | Once daily | Undiluted IM injection over 3 minutes |
| Acute Stroke | 20-50mL | Once daily for 10-21 days | IV infusion (diluted to 100mL minimum) |
| Traumatic Brain Injury | 20-50mL | Once daily for 7-30 days | IV infusion (diluted to 100mL minimum) |
| Alzheimer's Disease | 10-30mL | 5 days weekly for 4 weeks | IV injection/infusion (2-4 cycles yearly) |
| Vascular Dementia | 10-30mL | 5 days weekly for 4 weeks | IV injection/infusion (2-4 cycles yearly) |
Safe combination with no significant interactions; both support cognitive function.
No interactions reported; may have synergistic cognitive effects in Alzheimer's treatment.
Potential additive neurotropic effects; monitor for enhanced antidepressant effects.
May have additive neurological effects; requires careful monitoring.
Contraindicated per prescribing information; do not mix in same infusion.
Should not be mixed in same IV infusion per official guidelines.
Compatibility issues; do not mix in same IV infusion.
Both enhance neurotrophic factors; potential additive effects—start with lower doses.
Initial neuroprotective effects; possible mild side effects (dizziness, agitation)
Neurological improvements become apparent; cognitive function may begin to improve
Continued recovery; motor function improvements in stroke/TBI patients
Sustained benefits; cognitive enhancement plateaus in chronic conditions
The Cochrane database of systematic reviews · Ziganshina LE, Abakumova T, Hoyle CH
This Cochrane review assessed randomized trials in acute ischaemic stroke and reported no clear reduction in death or dependency, with concern about serious adverse events in the included evidence.
Stroke · Heiss WD, Brainin M, Bornstein NM, Tuomilehto J, Hong Z, Cerebrolysin Acute Stroke Treatment in Asia (CASTA) Investigators
This large randomized trial in acute ischemic stroke reported no significant overall difference on the primary 90-day global outcome between Cerebrolysin and placebo groups.
Stroke · Muresanu DF, Heiss WD, Hoemberg V, Bajenaru O, Popescu CD, Vester JC, Rahlfs VW, Doppler E, Meier D, Moessler H, Guekht A
This multicenter trial studied patients after ischemic stroke with motor impairment and reported higher 90-day motor-recovery scale scores in the Cerebrolysin group alongside standardized rehabilitation.
Journal of neuroscience research · Zhang C, Chopp M, Cui Y, Wang L, Zhang R, Zhang L, Lu M, Szalad A, Doppler E, Hitzl M, Zhang ZG
This experimental stroke study reported increased markers of neurogenesis and better functional outcome measures in animals receiving Cerebrolysin after focal cerebral ischemia.
European journal of neurology · Alvarez XA, Cacabelos R, Laredo M, Couceiro V, Sampedro C, Varela M, Corzo L, Fernandez-Novoa L, Vargas M, Aleixandre M, Linares C, Granizo E, Muresanu D, Moessler H
This randomized trial compared three Cerebrolysin dosing regimens with placebo in mild to moderate Alzheimer’s disease and reported dose-related differences on cognitive and global clinical scales.
Plain-English guides and study summaries from published literature.
The Neuroprotective Peptide Therapy Used for TBI, Stroke, and Cognitive Decline Research Traumatic brain injury, Alzheimer’s disease, stroke—these are some of the most life-altering conditions on earth. And the frustrating truth is that many traditional approaches are either limited, slow, or inconsistent.
Read articleUnderstanding Cerebrolysin: A Hidden Gem Cerebrolysin isn’t “new.” It’s been around far longer than most people realize—it just hasn’t been widely used in the places you’d expect, for the reasons you’d expect. Your most valuable asset is the three-pound universe between your ears. If that fails, everything fails. Cerebrolysin matters because it addresses the predictable ways the brain breaks down—at the mechanism level, not the symptom level.
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