Skip to content
Breathing, swallowing or vision problems: call the emergency services (15 or 112 in France).

Botulinum toxin comparison: long-acting or short-acting

The long-acting and the short-acting toxin work in the same way, but at a different pace: one acts more slowly and for longer, the other faster and for a shorter time. Neither is better than the other. This comparison sets out, row by row, what their official product information says.

Since July 2026, two families of botulinum toxins have been approved for aesthetic use in Europe9. This comparison builds on our page about what the new botulinum toxin is: it puts the two profiles side by side, based on their official product information, to help you prepare the discussion with your doctor.

Why a comparison without a winner?

It is tempting to look for "the best" toxin. The data do not allow it. There is no trial directly comparing type A toxin and the short-acting toxin: the pivotal trial of the latter has no active comparator, because no serotype E product was marketed yet10. Every comparison on this page therefore brings together product information drawn from different trials.

What can be said with certainty is that the two families do not have the same pace. The short-acting toxin gives you a choice between two profiles: one slower and longer-lasting, the other faster and shorter. Which one suits you depends on what you are looking for, the area to be treated and your medical situation.

The comparison table

Two families of toxins, two different profiles: one works faster and for a shorter time, the other more slowly and for longer. Neither is better than the other. The short-acting toxin gives you a choice, to be made with your doctor.

Comparison of the two families of botulinum toxins
CriterionLong-acting botulinum toxinType AShort-acting botulinum toxinSerotype E
First effects1,2,3,4Usually 2–3 days (up to one week)From 8 hours
Peak effect5,1,2,4Between week 2 and week 4Around day 7
Usual duration3,6,7,4Usually 3–4 months, up to 6 months depending on the product2–3 weeks
Approved aesthetic areas (France)3,2,8,4Frown lines; depending on the product, crow’s feet and forehead linesFrown lines only
Track record8,4Over 20 years of aesthetic use in France (first aesthetic approval: 2003)Approved in the European Union since July 2026
Treatment rhythm1,2,4Sessions at least 3 months apartOccasional use (as stated in the label)

No trial directly compares the two families of toxins: this table describes the data from their respective labels; it does not rank them.9

What each row means

First effects

With the short-acting toxin, clinical effects begin to show 8 hours after injection1. This is the first time point measured in the trials: the beginning of an effect, not a complete result. With type A toxins, first effects usually appear within 2 to 3 days2,4, and one product information states that the effect usually appears within one week3. For a detailed look at these timelines, see how long botulinum toxin takes to work.

Peak effect

The effect of the short-acting toxin peaks around day 71. That of type A toxins is reached, depending on the product, during the second week5 or around day 302,4. This is why the table gives "between week 2 and week 4" for type A2,5. In both cases, this is when the result can be assessed.

Usual duration

This is the clearest difference. The effect of the short-acting toxin usually lasts 2 to 3 weeks1. That of type A toxins lasts up to 4 months for most products2,3,4, and an effect has been shown for up to 6 months for some6,7. A short duration means that a result, expected or not, fades sooner; a long duration means less frequent sessions. The page on how long botulinum toxin lasts explains why the effect always wears off in the end.

Approved aesthetic areas

In France, all type A toxins for aesthetic use are approved for frown lines; depending on the product, some are also approved for crow’s feet and forehead lines3,4,7. The short-acting toxin is approved only for frown lines between the eyebrows in adults, when they have an important psychological impact1. Other areas of the face are not included in any of these aesthetic approvals.

Track record

The first aesthetic approval of a type A toxin in France dates from 20038, which means more than 20 years of use. The short-acting toxin has been approved in the European Union since 15 July 20269 and in Canada since 22 June 202611. A shorter track record does not mean a less safe product: it means fewer years of observation in everyday practice, and this toxin is also subject to additional monitoring9.

Treatment rhythm

The product information of type A toxins requires at least 3 months between two sessions2,4. That of the short-acting toxin provides for occasional use, because of its early onset and short duration1. Retreatment less than 6 weeks after the previous injection has not been evaluated, nor have more than 3 consecutive injections beyond 18 weeks1.

Long-acting or short-acting: what the table does not show

Three points do not fit in a table, but they matter in the decision.

Doses do not translate. Each product has its own unit of measurement, not interchangeable with that of the others1,2,4. Comparing "numbers of units" between two toxins therefore makes no sense.

Side effects cannot be compared directly. For the short-acting toxin, the trials report a drooping eyelid in 0.17% of patients, a drooping eyebrow in 0.13% and an upward lift of the outer end of the eyebrow in 0.04%1. The frequencies for type A toxins come from other trials, in other areas and at other doses: putting them side by side would be misleading.

Age is not a simple rule. Data on the short-acting toxin after 65 are limited1: only 7% of trial patients were in this age group, with lower response rates on day 71. But several type A toxins are not indicated after 65 either2,4,6, and one is indicated up to 755. It is for the doctor to judge.

When the long-acting toxin remains the right choice

The short-acting toxin does not make the long-acting toxin outdated. The authors of the phase 3 trial acknowledge it themselves: its shorter duration may be a disadvantage for people seeking a longer-lasting effect, and it is not intended for long-term use10. The block below sums up what the product information and the studies say.

Two profiles, a choice to make with your doctor

When the long-acting toxin remains the right choice

  • For a longer-lasting effect: usually 3–4 months, up to 6 months depending on the product, versus 2–3 weeks for the short-acting toxin.1,2,3,4
  • For long-term maintenance treatment: the short-acting toxin’s label specifies occasional use, and there are no data beyond 3 consecutive injections over 18 weeks.3,4
  • For crow’s feet and forehead lines: in France, only some type A toxins are approved for these areas; the short-acting toxin is approved for frown lines only.1,5,6,7,3
  • Over 65, to be discussed: data on the short-acting toxin are limited and response rates are lower in this age group. Several type A toxins are not indicated after 65 either: there is no simple rule, and the decision rests with the doctor.3,6,5,8
  • For less frequent sessions: at least 3 months between two type A sessions, whereas the short-acting toxin’s effect lasts 2–3 weeks.6,5,3

When the short-acting toxin may be discussed

  • For a first treatment, or when hesitant: this is the hypothesis put forward by the authors of the phase 3 study, which was funded by the manufacturer.4
  • To see the effect before a longer-lasting treatment: the same authors describe it as a "trial" treatment. A type A toxin injected less than 30 days afterwards has not been evaluated.4,3
  • For a rapid effect: first effects from 8 hours, peak effect around day 7.3

These are general pointers. The choice of toxin, and the decision whether or not to be treated, are made in consultation with your doctor.

Switching from one family to the other

Switching from a type A toxin to the short-acting toxin, or the other way round, is a decision for the doctor, who then sets a new dose. The product information of the short-acting toxin states that a type A toxin injected less than 30 days after it has not been evaluated1. In a phase 1 study, a type A toxin injected on day 30 had a similar effect whether the subjects had previously received this toxin or a placebo1. The same product information states that it must not be given at the same time as another botulinum toxin, a combination that has not been studied1.

The practical questions raised by any change of product, whatever the family, are covered in our article on switching botulinum toxin. The trials behind these figures, and the questions that remain open, are detailed on the page what the studies say about the new botulinum toxin.

Key points

  • Same mechanism, different pace: the short-acting toxin works faster and for a shorter time than type A toxin1,3.
  • Usual duration: 2 to 3 weeks for the short-acting toxin, usually 3 to 4 months for type A, up to 6 months depending on the product1,3,6.
  • A single approved area for the short-acting toxin, frown lines; type A also covers, depending on the product, crow’s feet and the forehead1,3.
  • No trial directly compares the two families: this comparison does not name a winner10.
  • The choice is made during a consultation, with your doctor.

Frequently asked questions

  • What is the main difference between the long-acting toxin and the short-acting toxin?

    Their pace. Both block the same protein inside the nerve ending1,3,4, but the short-acting toxin works faster and for a shorter time: first effects from 8 hours, peak effect around day 7, duration of 2 to 3 weeks1. Type A toxin usually starts working within 2 to 3 days, reaches its peak between week 2 and week 4 and usually lasts 3 to 4 months2,4.

  • Which one is more effective?

    No study allows us to say. There is no trial directly comparing the two families of toxins: the phase 3 trial of the short-acting toxin was run against placebo, because no serotype E product was marketed yet10. The efficacy figures in each product information come from different trials and cannot be set side by side to pick a winner.

  • Can a type A toxin be injected right after the short-acting toxin?

    A type A toxin injected less than 30 days after the short-acting toxin has not been evaluated1. In a study of 90 subjects, a type A toxin injected on day 30 had a similar effect whether the subjects had previously received the short-acting toxin or a placebo1. The timing is decided with your doctor.

  • Are doses the same from one product to another?

    No. Each botulinum toxin has its own unit of measurement, and the product information states that these units are not interchangeable with those of other products1,2,4. An effective dose with one toxin therefore says nothing about the dose needed with another. This is one of the reasons why the choice of product and dose lies with the doctor.

Sources

  1. 1.Summary of product characteristics of the serotype E botulinum toxin approved in the European Union (EPAR annex I) (opens in a new tab) — European Commission (Union Register of medicinal products)
  2. 2.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 66865211) (opens in a new tab) — French public medicines database (BDPM)
  3. 3.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 68150775) (opens in a new tab) — French public medicines database (BDPM)
  4. 4.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 61592762) (opens in a new tab) — French public medicines database (BDPM)
  5. 5.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 69878363) (opens in a new tab) — French public medicines database (BDPM)
  6. 6.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 69497348) (opens in a new tab) — French public medicines database (BDPM)
  7. 7.SmPC of a type A botulinum toxin approved for aesthetic use in France (BDPM, CIS 65066375) (opens in a new tab) — French public medicines database (BDPM)
  8. 8.French public medicines database: list of medicinal products (CIS file), updated 29 September 2026 (opens in a new tab) — French public medicines database (Ministry of Health)
  9. 9.European public assessment report (EPAR) of the serotype E botulinum toxin (opens in a new tab) — European Commission (Union Register of medicinal products)
  10. 10.Lain E. et al., pivotal phase 3 trial of a serotype E botulinum toxin for glabellar lines, Aesthetic Surgery Journal, 2026 (manufacturer-funded study) (opens in a new tab) — Aesthetic Surgery Journal (Oxford University Press)
  11. 11.Canadian product monograph of the serotype E botulinum toxin (authorization date: 2026-06-22) (opens in a new tab) — Health Canada
SOS after an injection