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(az-fi-sell tee) ,


(trade name)


Therapeutic: cosmetic agents
Pharmacologic: temporary class
Pregnancy Category: C


To improve the appearance of moderate to severe wrinkles in the nasolabial fold.


Cells are obtained from patient's post-auricular skin. These dernmal fibroblasts are then prepared and injected into nasolabial folds.

Therapeutic effects

Decreased nasolabial fold wrinkles.


Absorption: Unknown.
Distribution: Unknown.
Metabolism and Excretion: Unknown.
Half-life: Unknown.

Time/action profile (improvement in appearance)

Intradermal4–5 mounknownunknown


Contraindicated in: Previous hypersensitivity to azficel-T; Hypersensitivity to amphotericin, dimethyl sulfoxide (DMSO), gentamicin or materials of bovine origin; Known history of keloid or excessive scar formation; Acute local skin infection ( may cause spread).
Use Cautiously in: Genetic disorders affecting dermal fibroblasts or formation of normal collagen matrices (abnormal responses may occur);Concurrent immunosuppressants, radiation, chemotherapy or immunomodulatory therapy (↑ risk of infection with ↓ healing);Concurrent use of anticoagulants (↑ risk of bleeding); Obstetric: Use in pregnancy only if clearly needed; Pediatric: Safe and effective use in children has not been established.

Adverse Reactions/Side Effects


  • erythema (most frequent)
  • bruising (most frequent)
  • edema (most frequent)
  • bleeding
  • dermatitis
  • irritation
  • nodules
  • papules
  • pruritus
  • redness
  • keloid/hypertrophic scarring


  • hypersensitivity reactions including analphyaxis (life-threatening)
  • basal cell cancer
  • herpes labialis
  • vasculitis


Drug-Drug interaction

Concurrent use of antineoplastices, immunosuppressants and immunomodulators ↑ risk of infection and poor healing.Concurrent use of anticoagulants ↑ risk of bleeding.


Intradermal (Adults) 0.1 mL/linear centimeter into nasolabial fold wrinkles. Course is three treatment sessions (up to 2 mL/session) at 3–6 wk intervals.


Suspension for autologous intradermal injection: 18 million autologous fibroblasts/1.2 mL sufficient to deliver 1 mL of product

Nursing implications

Nursing assessment

  • Monitor for signs and symptoms of allergic reactions (difficulty breathing, trouble swallowing, rash, hives, severe redness, swelling) during and following injections. Stop injections and treat symptomatically.

Potential Nursing Diagnoses

Disturbed body image (Indications)


  • Only health care professional completing a Fibrocell-approved training program should administer azficel-T.
  • Intradermal: Azficel-T is made when 3 small skin biopsies are taken from behind patient ears and sent to manufacturer. Certain cells, called fibroblasts, are grown from samples taking 3–6 mo. Once grown and returned, health care professional matches patient to azficel-T vial to patient unique identifier and cells are injected into nasolabial fold in 3 sessions, 3–6 mo apart.
  • Allow vial to reach room temperature 15–30 min. Gently invert to re-suspend; tap vial to release fluid retained in top. Do not dilute. Prepare 4 sterile 0.5 mL syringes with 21-gauge needles; replace with 30-gauge needle for injections.
    • Make sure injection areas are free from hair, cosmetics, or facial jewelry.
    • Evaluate need for topical anesthesia; do not use injectable local anesthetics.
    • After injection, leave treated area undisturbed. Do not rub, massage or compress area. Apply a cold pack for 2–3 minutes. Do not place ice directly against skin.

Patient/Family Teaching

  • Explain purpose and procedure for azficel-T. Inform patient of importance of treatment schedule. If a treatment session is missed, cells will expire and must be thrown out, so new treatment sessions must be scheduled. Also, there is a chance that skin samples will not make enough cells to use. If this occurs, new biopsies may need to be taken.
  • Advise patient on post-treatment care. Do not apply ice to face; cold compress may be applied for 2–3 minutes at a time, if needed to ease swelling or discomfort. For at least 24 hours, do not wash site of injections. Do not scrub, rub or manipulate treatment area for at least 72 hours. Do not apply any products (make-up, facial creams, sunscreen) to treatment area for 72 hr.
  • Inform patient of what to expect post-procedure. Expect mild to moderate redness, swelling, puffiness, or bruising following injections. Advise patient to call doctor or emergency department for any persistent or unexpected side effects.
  • Instruct patient to notify health care provider if fever over 100°F, redness, warmth, or pain at injection or biopsy sites lasts more than 3 days.
  • Instruct patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to avoid concurrent use of Rx, OTC, and herbal products without consulting health care professional.

Evaluation/Desired Outcomes

  • Decreased nasolabial fold wrinkles. Effects are not immediate, but may appear over course of the three-treatment regimen.
Drug Guide, © 2015 Farlex and Partners
References in periodicals archive ?
Laviv et al., "The malignant potential of endometrial polyps," European Journal of Obstetrics & Gynecology and Reproductive Biology, vol.
The experiments were done at the Laboratory of Plant Pathology (LAVIV), and at the greenhouse of the Instituto de Ciencias Agrarias da Universidade Federal de Uberlandia (UFU) and on a commercial passion fruit farm in Cruzeiro dos Peixotos, municipality of Uberlandia, MG.
[7] Liran Levin, Amir Laviv and Devorah Schwartz-Arad, 2006.
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Fibrocell's technology led to the FDA-approved cell based autologous fibroblast product, azficel-T (LAVIV).
Shamasna's lawyer Laviv Habib told Israeli newspaper Haaretz that the fact that the IDF took so long to declare that Shamasna's shooting took place during a military operation showed a lack of integrity.
The company's LAVIV (azficel-T) is the first and only Food and Drug Administration (FDA)-approved personalised cell therapy for aesthetic use.
Now, the company plans to concentrate on the commercialisation of its lead product LAVIV, which recently got the green light from the US Food and Drug Administration, Fibrocell's chairman and CEO David Pernock said, explaining the decision for the move.
If these new products are approved in 2012, they will provide patients with yet another option in a year of options." Finally, new fillers, such as Belotero A and LaViv A will offer increased choice to both physicians and patients in the dermal filler arena.
M2 PHARMA-November 4, 2011-Fibrocell Science unveils study data for LAVIV in depressed acne scars(C)2011 M2 COMMUNICATIONS
LaViv has been found to banish lines with no side effects and has been licensed in the Us.
The new drug, laViv, has been proven to improve the appearance of smile lines and doesn't paralyse the face like Botox does.