Can Depo-Provera (medroxyprogesterone acetate) cause breast cellulitis in a female of reproductive age with no significant past medical history?

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Depo-Provera Does Not Cause Breast Cellulitis

Depo-Provera (depot medroxyprogesterone acetate/DMPA) does not cause breast cellulitis. This is not a recognized side effect of this contraceptive method in any of the established medical literature or FDA guidance.

Known Side Effects of Depo-Provera

The documented side effects of DMPA are well-established and do not include breast cellulitis or breast infections:

  • Common side effects include menstrual irregularities (with 57% experiencing amenorrhea by one year), weight gain, headache, nervousness, abdominal discomfort, dizziness, and asthenia 1
  • Breast-related effects are limited to breast tenderness, which is a recognized but uncommon side effect 2
  • Women using DMPA for several years do not observe changes in breast size, and the method does not cause breast tissue inflammation or infection 3

Mechanism of Action

DMPA works through multiple mechanisms that have no relationship to breast tissue infection:

  • Inhibits ovulation by suppressing the midcycle LH peak 3
  • Causes endometrial atrophy 3
  • Thickens cervical mucus 3
  • Maintains serum estradiol levels in the early to midfollicular phase range (mean approximately 50 pg/mL) 3

Safety Profile

The extensive safety data on DMPA, used by over 90 million women worldwide, has established that:

  • DMPA does not increase risk of cardiovascular events, breast cancer, other gynecologic malignancy, or postmenopausal fracture 4
  • The method has no appreciable effects on blood pressure or thrombosis risk 5
  • Contraindications include undiagnosed vaginal bleeding, known or suspected breast malignancy, thromboembolic disorders, cerebral vascular disease, and liver dysfunction—but not conditions related to breast infections 1

Clinical Implication

If a patient develops breast cellulitis while using Depo-Provera, investigate other causes. Breast cellulitis typically results from:

  • Bacterial skin infection (most commonly Staphylococcus aureus or Streptococcus species)
  • Trauma or breaks in skin integrity
  • Mastitis (in lactating women)
  • Underlying breast conditions

The temporal association with Depo-Provera use would be coincidental rather than causal.

References

Research

3-month contraceptive injection approved.

FDA medical bulletin : important information for health professionals from the U.S. Food & Drug Administration, 1993

Research

Injectable contraception.

Clinical obstetrics and gynecology, 2007

Research

Pharmacokinetics of depot medroxyprogesterone acetate contraception.

The Journal of reproductive medicine, 1996

Research

Depot-medroxyprogesterone acetate: an update.

Archives of gynecology and obstetrics, 2008

Research

Depo Provera. Position paper on clinical use, effectiveness and side effects.

The British journal of family planning, 1999

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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