RISKS, SIDE EFFECTS AND CONTRAINDICATIONS

AESTHETIC DOCTORS MEXICO

Risks and Possible Side Effects

Pain, bruising, edema, and pruritus (swelling and skin irritation/itching) at the injection site.
Cephalalgia (headache).
Asthenia, fatigue, general malaise or flu-like symptoms.
Temporary muscle weakness in muscles near the application site.
Temporary facial asymmetry.
Eyelid ptosis or drooping eyebrow (temporary).
Musculoskeletal pain.
Dysphagia – difficulty swallowing (rare).
Neuralgic amyotrophy (rare) – a rare neurological disorder that causes severe pain, muscle weakness, and muscle wasting, usually in the shoulder or arm.
Skin reactions: itching, redness, or rashes.
Insufficient results or a shorter-than-expected duration.
A very rare risk of systemic toxin spread, which may lead to paralysis, dysphonia, respiratory distress, or aspiration pneumonia.
Reduction of blinking, ocular dryness and visual discomfort when applied in the periocular region.

Contraindications

Pregnancy and lactation.
Myasthenia gravis.
Eaton-Lambert syndrome.
Hypersensitivity to botulinum toxin type A or excipients.
Active infection in the area of application.

DERMAL FILLERS

(Hyaluronic Acid / Calcium Hydroxyapatite in volumetric doses)

Risks and Possible Side Effects

Pain, bruising, edema (swelling), and redness.
Temporal asymmetries.
On over- or under-correction of volume.
Irregularities, palpable nodules, indurations, or granulomas (small lumps or swellings that appear some time after the procedure).
Product migration.
Rare allergic reactions.
Local infection.
Rare vascular risks, including vascular occlusion, ischemia, necrosis, and, in extremely rare cases, cerebrovascular events, visual disturbances, or blindness.

Contraindications

Pregnancy and lactation.
Allergy to hyaluronic acid, calcium hydroxyapatite, or lidocaine.
Infection or active herpes.
Decompensated autoimmune diseases.
Uncontrolled coagulation disorders.

COLLAGEN BIOSTIMULATION

(Radiesse® / Sculptra®)

Risks and Possible Side Effects

Local pain and discomfort.
Edema (swelling), bruising, and redness.
Induration, palpable or visible nodules.
Sensation of tightness.
Late-onset granulomas (small lumps or swellings that appear some time after the procedure).
Infection.
Temporal asymmetries.
Herpes reactivation in susceptible patients.
Results may vary depending on individual response.
Multiple sessions may be necessary to achieve optimal results.

Contraindications

Pregnancy and lactation.
Active autoimmune or collagen diseases.
Allergy to components.
Infection in the area of application.

PB SERUM ENZYMES

(1st and 2nd generations)

Risks and Possible Side Effects

Pain or burning during and after the procedure.
Common symptoms of the flu: headache, fever, muscle aches.
Bruises and edema (swelling)
Redness and pruritus (irritation or itching)
Local inflammation.
Punctate small scabs.
Allergic reaction.
Local infection.
Temporary changes in pigmentation.
Prolonged inflammation.
Results may vary or be unpredictable depending on the individual’s response.

Contraindications

Pregnancy and lactation.
Allergy to components.
Infection or local active dermatitis.
Uncontrolled coagulation disorders.

SKINBOOSTER AND NCTF

(Restylane® Skinboosters Vital / Vital Light)

Risks and Possible Side Effects

Hematoma or ecchymosis.
Erythema.
Pruritus.
Immediate or delayed swelling or edema (swelling).
Spontaneous pain or pain on palpation.
Temporal asymmetries.
Nodules or indurations.
Infection.
Rare allergic reactions.
On overcorrection or undercorrection.
Rare vascular risks, including vascular occlusion, ischemia, necrosis, and, in extremely rare cases, cerebrovascular events, visual disturbances, or blindness.

Contraindications

Pregnancy and lactation.
Allergy to hyaluronic acid or lidocaine.
Active infection or herpes.

GENEO+ MEDICAL AND FACIAL PEELS

Risks and Possible Side Effects

Mild allergic reactions.
Redness, irritation and burning sensation.
Bruises and edema (swelling).
Small scabs.
Mild to moderate desquamation.
Increased sensitivity to sunlight following the procedure.
Pigmentation changes: hyper- or hypopigmentation.
Reactivation of herpes in predisposed persons.
Infection if improperly handled.

Contraindications

Pregnancy and lactation.
Allergy to ingredients.
Active infection or irritation.
Severe dermatitis.

NANOPORE / MICRONEEDLING

(with or without exosomes)

Risks and Possible Side Effects

Pain, erythema (redness of the skin), and edema (swelling).
Hematomas.
Pruritus.
Scabs.
Risk of bacterial or viral infection.
Reactivation of herpes.
Hypo- or hyperpigmentation (may be permanent).
Hypertrophic scarring or keloids in predisposed patients.
Sensitivity and desquamation.
Posterior intense photosensitivity.
Temporary acne-like breakouts.
Results may vary depending on skin type and aftercare.

Contraindications

Active herpes.
Tendency to keloids.
Infection in the area.
Active dermatological diseases.
Pregnancy and breastfeeding, based on clinical judgment.

VENUS LEGACY

(Radio Frequency + Electromagnetic Fields)

Risks and Possible Side Effects

Redness and local heat.
Edema (swelling).
Hematomas.
Sensitivity or temporary pain in the back.
Temporary changes in skin texture.
Blisters (rare).
Changes in pigmentation (hyperpigmentation or hypopigmentation).
Low risk of burns.
Results may vary depending on the patient’s individual condition.

Contraindications

Pregnancy.
Pacemakers or implanted electronic devices.
Metal implants near the treatment area.
Active infection or irritation in the area.
Severe alteration of sensitivity.

PDRN / SALMON POLYNUCLEOTIDES

(Salmon DNA / Polynucleotides)

Risks and Possible Side Effects

Pain, burning, or tenderness at the application site.
Temporary erythema (redness of the skin) and edema (swelling).
Bruises or ecchymosis.
Papules or small, temporary raised areas following application.
Itching or local irritation.
Temporary inflammation.
Allergic or hypersensitivity reactions (rare), especially in patients with an allergy to fish or shellfish.
Temporary acne-like breakouts.
Late-onset nodules or granulomas—small lumps or swellings that appear some time after the procedure (very rare).
Local infection.
Results vary depending on individual response and follow-up care.

Contraindications

Pregnancy and lactation.
An allergy test is required if you already have a preexisting condition involving allergies to fish and shellfish, although there are cases where there are no contraindications because the molecule is highly purified.
Active infection in the area of application.
Active dermatitis or significant skin conditions.
Decompensated autoimmune diseases.
Uncontrolled coagulation disorders.

LIFTERA®

(High-Intensity Focused Ultrasound – HIFU)

Risks and Possible Side Effects

Temporary redness.
Mild or moderate edema (swelling).
A sensation of heat, burning, or tenderness after treatment.
Temporary pain or discomfort during the procedure.
Tingling or temporary increased sensitivity.
Occasional bruising.
Temporary numbness or mild changes in sensation.
Temporary changes in skin texture.
Hypopigmentation or hyperpigmentation (rare).
Superficial burns or blisters (very rare).
Temporal asymmetries.
Results may vary depending on the patient’s individual characteristics.
Multiple sessions or periodic maintenance may be necessary.

Contraindications

Pregnancy and lactation.
More than three metal dental implants (the ones with screws).
Pacemakers or implanted electronic devices.
Metal implants in the treatment area.
Infection, open wounds, or active irritation in the area.
Severe acne or active skin conditions.
Severe sensory disturbances.
Epilepsy or uncontrolled neurological disorders.
Decompensated systemic diseases, as determined by a physician.

RESULTS AND EXPECTATIONS

Results may vary depending on each patient’s individual characteristics, age, metabolism, lifestyle, post-treatment care, and adherence to medical instructions.
No procedure guarantees results that are exact, permanent, or identical to personal expectations.
Some procedures may require additional sessions or periodic maintenance to maintain the expected results.

AFTERCARE AND PATIENT RESPONSIBILITY

Follow your doctor’s post-procedure instructions.
Avoid touching or massaging the treated areas, unless otherwise directed by a doctor.
Avoid direct sun exposure and use appropriate sunscreen.
Report any unusual symptoms, severe pain, changes in color, vision problems, or signs of infection immediately.
Failure to follow post-treatment care instructions can affect outcomes and increase the risk of complications.

Every cosmetic medical procedure involves risks, potential side effects, and variable results, even when performed correctly and in accordance with appropriate medical protocols.