Non-randomised trial, 2024
Is a combination of naproxen, paracetamol, and pamabrom safe and effective for PMS?
Yes, this combination was safe and effective. Only 3% of women experienced adverse events, and 70.7% achieved at least 50% reduction in pain.
What they did
Prospective observational study in routine clinical practice from December 2017 to December 2019. 270 women older than 18 years with PMS received a fixed-dose tablet containing naproxen 220 mg, paracetamol 300 mg, and pamabrom 25 mg. Researchers tracked adverse events, pain intensity, and PMS symptoms across multiple centers.
What they found
Eight out of 270 women (3%) experienced adverse events: headache (5 cases), gastritis (2), dyspepsia (1), diarrhea (1), and nausea (1). Pain intensity decreased significantly with a median reduction of 4.5 points. 70.7% of women achieved at least 50% pain reduction.
What it means for you
This three-drug combination is a safe and effective option for PMS pain and symptoms, with low adverse event rates. However, this was an observational study without a control group or blinding, so we cannot be certain the medication alone caused the improvement.
270
women in study
3%
experienced adverse events
70.7%
achieved 50% or greater pain reduction
About the study
- Original title
- Safety and Effectiveness of Naproxen 220 mg + Paracetamol 300 mg + Pamabrom 25 mg Fixed Dose Combination in Women with Premenstrual Syndrome: A Post-Marketing, Open-Label, Uncontrolled, Prospective, Multicenter, Observational Study
- Authors
- Álvaro Eduardo Peña-Jiménez, Omar Benítez-Aguilar, Jesús E. Villegas et al.
- Journal
- Women
- Year
- 2024
- Study design
- Non-randomised trial
- Participants
- 270
- What was tested
- Fixed-dose combination tablet: naproxen 220 mg, paracetamol 300 mg, and pamabrom 25 mg
- Open access
- Yes
- Read the paper
- doi.org/10.3390/women4010002
Original abstract
Premenstrual syndrome is characterized by pain and symptoms affecting the women´s quality of life. We aimed to evaluate the safety and effectiveness of an oral fixed dose combination containing naproxen 220 mg + paracetamol 300 mg + pamabrom 25 mg tablet (Analgen Fem®) during the routine clinical practice. A prospective, open-label, multicenter, observational post-marketing study was conducted from December 2017 to December 2019 including 270 women older than 18 years. Primary endpoint was the proportion of adverse events, meanwhile the pain intensity, premenstrual syndrome symptoms, and patient proportion with a pain score reduction by at least 50% were secondary endpoints. The mean age of population was 28.9 ± 8.8 years. Among the 270 women, 8 (3%) experienced 10 adverse events. These were headache (5/8), gastritis (2/8) dyspepsia (1/8), diarrhea (1/8) and nausea (1/8). The investigator discontinued the study medication in 3/8 patients because of adverse events. The median of differences between the pain intensity at baseline and at last observation (-4.5, 95%CI; -5, -4) demonstrated that naproxen 220 mg + paracetamol 300 mg + pamabrom 25 mg fixed dose combination reduced pain intensity (p<0.001). In addition, the proportion of patients with pain reduction by at least 50% at the end of the treatment was 70.7%. The study demonstrated that this drug represents a safe and tolerated treatment, reducing pain intensity and premenstrual symptoms.
Reproduced under CC-BY.
Topics
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