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Progestogen (anti-mineralocorticoid, anti-androgenic) Pregnancy: Should not be used during pregnancy — if pregnancy occurs during treatment, further intake should be stopped. Epidemiological studies have revealed neither an increased risk of birth defects in children born to women who used drospirenone prior to pregnancy, nor a teratogenic effect when it was taken inadvertently during pregnancy; animal studies have shown reproductive toxicity, so undesirable effects due to the hormonal action of the active compound cannot be excluded. Breastfeeding: negligible amounts of drospirenone are excreted in breast milk (the daily dose in the baby is less than 1% of the maternal dose) and no effects on breastfed newborns/infants are anticipated at therapeutic doses — based on available data it may be used during lactation.

Drospirenone

Brand names: Slynd (POP), Yasmin (with EE), Yaz (with EE), Eloine (with EE), Lucette (with EE)

Drospirenone is a progestogen with anti-mineralocorticoid and anti-androgenic activity, used in combined hormonal contraceptives and as a progestogen-only contraceptive pill.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: One tablet daily for 28 consecutive days — one white active tablet (4 mg drospirenone) daily during the first 24 days, then one green inactive tablet daily during the 4 following days
Route: Oral
Frequency: Once daily at about the same time of day so that the interval between two tablets is always 24 hours; tablet taking is continuous, with a subsequent pack started immediately after finishing the previous pack without a break
Fetched label is 'Slynd 4mg film-coated tablets' (UK SPC) — a progestogen-only contraceptive. Tablets should be taken in the order shown on the blister; day-of-week stickers are provided. STARTING: with no preceding hormonal contraceptive use in the past month, the first tablet should be taken on day 1 of the natural cycle (first day of menstrual bleeding) and no additional contraceptive measures are necessary. Following first-trimester abortion, start immediately after the abortion took place with no additional contraceptive method needed. Following delivery or second-trimester abortion, start between 21 and 28 days afterwards; if started later but before menstruation has returned, pregnancy must be ruled out and an additional method of contraception used for the first week. Changing from a combined hormonal contraceptive: start preferably on the day after the last active tablet of the previous COC or on the day of removal of the vaginal ring or transdermal patch (no additional contraceptive necessary); if starting at the latest on the day following the usual hormone-free or placebo interval, an additional barrier method is recommended for the first 7 days. Changing from another progestogen-only pill: start the day after, within 24 hours of discontinuing the previous POP; from an implant or IUS, on the same day it is removed; from an injectable, on the day the next injection was due — in all of these cases no additional contraceptive is necessary. MISSED TABLETS: if less than 24 hours late in taking any single tablet, contraceptive protection is not reduced — take the tablet as soon as remembered and take further tablets at the usual time. If more than 24 hours late in taking any white active tablet, contraceptive protection may be reduced and a barrier method such as a condom should be considered for the next 7 days; take the missed tablet as soon as remembered, even if this means taking two tablets at the same time, then continue at the usual time. If tablets were missed in the first week after initiation and intercourse took place in the week before, the possibility of pregnancy should be considered. If tablets were missed in the third week of pill taking, take the last missed tablet as soon as remembered (even if two tablets at once), continue the active tablets at the usual time, and then do not take the placebo tablets — continue straight on to the next active blister pack. Missed green placebo tablets can be disregarded but should be discarded to avoid unintentionally prolonging the interval between active tablets. GASTROINTESTINAL DISTURBANCE: if vomiting or diarrhoea occurs within 3-4 hours after tablet taking, take a new replacement tablet as soon as possible, ideally within 24 hours of the usual time; if more than 24 hours elapse, apply the missed-tablet advice. HYPERKALAEMIA: drospirenone is an aldosterone antagonist with potassium-sparing properties — check serum potassium levels during the first treatment cycle in women with renal insufficiency and pre-treatment serum potassium in the upper reference range, and during concomitant use of potassium-sparing medicinal products. Paediatric (non per-kg, so not expressed as a mg/kg dose): safety and efficacy have been established in women of reproductive age and are expected to be the same for post-pubertal adolescents under the age of 18; use before menarche is not indicated. Verify any under-18 use against a children's formulary.

Dose adjustments

Renal

Contraindicated in severe renal insufficiency or acute renal failure. In women with renal insufficiency (and pre-treatment serum potassium in the upper reference range) it is recommended to check serum potassium levels during the first treatment cycle, because drospirenone is an aldosterone antagonist with potassium-sparing properties. No numerical dose adjustment is stated.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Active venous thromboembolic disorder
  • Presence or history of severe hepatic disease as long as liver function values have not returned to normal
  • Severe renal insufficiency or acute renal failure
  • Known or suspected sex-steroid sensitive malignancies
  • Undiagnosed vaginal bleeding
  • Hypersensitivity to the active substance or to any of the excipients

Side effects

  • Changes in the bleeding pattern — metrorrhagia (2.9%), vaginal haemorrhage, irregular menstruation, amenorrhoea
  • Acne (3.8%)
  • Headache (2.7%)
  • Breast pain / breast discomfort (2.2%)
  • Nausea, abdominal pain; weight increased; fatigue
  • Libido disorder, mood disturbances, depressed mood; hyperkalaemia (uncommon)

Interactions

  • Potassium-sparing medicinal products — drospirenone is an aldosterone antagonist with potassium-sparing properties; check serum potassium levels during the first treatment cycle with concomitant use, and in women with renal insufficiency and pre-treatment serum potassium in the upper reference range (§4.4, cross-referencing §4.5)
  • NOTE: the UK SPC §4.5 interactions section was NOT captured in the fetched bundle — clinician to check the SPC §4.5 (including enzyme inducers and contraceptive efficacy) before sign-off

Clinical monograph

How it works

It provides contraception chiefly by inhibiting ovulation, with additional effects on cervical mucus and the endometrium; its anti-mineralocorticoid action counteracts oestrogen-related fluid retention.

Prescribing in practice

  • Because of its anti-mineralocorticoid effect, use caution and consider potassium monitoring when co-prescribed with other potassium-raising drugs, as hyperkalaemia can occur.
  • When used in a combined preparation, the standard venous thromboembolism risks and contraindications of combined hormonal contraception apply.
  • The progestogen-only drospirenone pill provides an oestrogen-free option with a more forgiving missed-pill window than older progestogen-only pills.

Monitoring

Monitor blood pressure; consider checking serum potassium in women also taking other agents that raise potassium or with relevant renal impairment.

Counselling the patient

  • Take the pill regularly as directed and follow missed-pill advice for your specific product.
  • Report symptoms of a blood clot such as calf swelling, breathlessness or chest pain promptly.
  • Tell your clinician about other medicines, particularly those affecting potassium levels.

Evidence & guidelines

Drospirenone-containing contraceptives are established options within UK contraceptive guidance, with attention to thromboembolic and potassium-related considerations.

Reference: SmPC Slynd / Yasmin / Yaz; FSRH UK MEC 2016 (amended 2019); MHRA Drug Safety Update Feb 2014 (COCs and VTE); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.