Click a topic to learn more about the following birth control side effects:
Birth control side effects
Many women dislike the idea of ingesting artificial hormones or of having devices implanted in their bodies. Increasingly, the effects of hormonal birth control and other forms of contraception on women’s health and wellbeing are becoming more evident.
Some of the side effects resulting from the use of hormonal contraceptives include:
- loss of libido
- rashes
- discoloration of the skin (melasma/chloasma)
- changes in weight or appetite
- nausea, vomiting
- migraines
- mood changes, including depression
- aggravation of varicose veins
- gastrointestinal symptoms (pain, cramps, bloating)
- spotting
- vaginitis (yeast infection)
- vitamin deficiencies
- water retention
- vision impairment
- liver malfunction (jaundice)
Further, numerous studies show increased risk of cancer and increased risk of blood clots resulting from the use of hormonal contraceptives.
Thousands of lawsuits have been filed in recent years against manufacturers of various birth control pills for serious health complications suffered, including:
- Heart attack
- Stroke
- Deep vein thrombosis (blood clots in legs)
- Pulmonary embolism (blockages in the lungs)
- Gallbladder disease
Likewise, thousands of women have filed claims against the manufacturers of the Mirena® IUD (intrauterine devices) for serious side effects. In general, IUDs increase risk of:
- Ectopic pregnancy (tubal pregnancy)
- Pelvic inflammatory disease
- Abnormal bleeding
- Infection
- Displacement of the device, which can lead to serious complications.
So many women reported adverse reactions to the Essure® sterilization procedure that its manufacturer paid out $1, 600,000,000 to settle claims of damages and it was pulled from the market in 2018.
Users of the copper IUD Paragard® have reported symptoms of copper toxicity.
To learn more about birth control side effects, see the articles below.
Women seeking to avoid birth control side effects can learn more about fertility awareness methods as natural alternatives to pharmaceutical birth control.
Mirena, Essure are registered trademarks of Bayer. Paragard is a registered trademark of CooperSurgical, Inc.
References
Click a subtopic below to view scientific references for each of the following items and their connections to birth control use.
CROHN’S DISEASE
Boyko EJ, Theis MK, Vaughan TL, and Nicol-Blades B. Increased risk of inflammatory bowel disease associated with oral contraceptive use. American Journal of Epidemiology 1994; 140:268–278.
Calkins BM, Mendeloff AI, and Garland C. Inflammatory bowel disease in oral contraceptive users. Gastroenterology 1986; 91: 523–524.
Cornish JA, Tan E, Simillis C, Clark SK, Teare J, and Tekkis PP. The risk of oral contraceptives in the etiology of inflammatory bowel disease: a meta-analysis. American Journal of Gastroenterology 2008; 103:2394–2400.
Corrao G, Tragnone A, Caprilli R, Trallori G, Papi C, Andreoli A, Di Paolo M, Riegler G, Rigo GP, Ferraù O, Mansi C, Ingrosso M, and Valpiani D. Risk of inflammatory bowel disease attributable to smoking, oral contraception and breastfeeding in Italy: a nationwide case-control study. Cooperative Investigators of the Italian Group for the Study of the Colon and the Rectum (GISC). International Journal of Epidemiology 1998; 27:397–404.
García Rodríguez LA, González-Pérez A, Johansson S, and Wallander MA. Risk factors for inflammatory bowel disease in the general population. Alimentary Pharmacology & Therapeutics 2005; 22:309–315.
Godet PG, May GR, and Sutherland LR. Meta-analysis of the role of oral contraceptive agents in inflammatory bowel disease. Gut 1995; 37:668–673.
Halfvarson J, Jess T, Magnuson A, Montgomery SM, Orholm M, Tysk C, Binder V, and Järnerot G. Environmental factors in inflammatory bowel disease: a co-twin control study of a Swedish-Danish twin population. Inflammatory Bowel Disease 2006; 12:925–933.
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Khalili H, Higuchi LM, Ananthakrishnan AN, Richter JM, Feskanich D, Fuchs CS, and Chan AT. Oral contraceptives, reproductive factors and risk of inflammatory bowel disease. Gut 2013; 62:1153–1159.
Lashner BA, Kane SV, and Hanauer SB. Lack of association between oral contraceptive use and Crohn’s disease: a community-based matched case-control study. Gastroenterology 1989; 97:1442–1447.
Lesko SM, Kaufman DW, Rosenberg L, Helmrich SP, Miller DR, Stolley PD, and Shapiro S. Evidence for an increased risk of Crohn’s disease in oral contraceptive users. Gastroenterology 1985; 89:1046–1049.
Logan RF and Kay CR. Oral contraception, smoking and inflammatory bowel disease—findings in the Royal College of General Practitioners Oral Contraception Study. International Journal of Epidemiology 1989; 18: 105–107.
Lowe AM, Roy PO, Poulin M, Michel P, Bitton A, St-Onge L, and Brassard P. Epidemiology of Crohn’s disease in Quebec, Canada. Inflammatory Bowel Disease 2009; 15:429–435.
Ng SC, Woodrow S, Patel N, Subhani J, and Harbord M. Role of genetic and environmental factors in British twins with inflammatory bowel disease. Inflammatory Bowel Disease 2012; 18:725–736.
Persson PG, Leijonmarck CE, Bernell O, Hellers G, and Ahlbom A. Risk indicators for inflammatory bowel disease. International Journal of Epidemiology 1993; 2(2):268–272.
Sandler RS, Wurzelmann JI, and Lyles CM. Oral contraceptive use and the risk of inflammatory bowel disease. Epidemiology 1992; 3:374–378.
Vcev A, Pezerovic D, Jovanovic Z, Nakic D, Vcev I, and Majnarić L. A retrospective, case-control study on traditional environmental risk factors in inflammatory bowel disease in Vukovar-Srijem County, north-eastern Croatia 2010. Wiener Klinische Wochenschrift 2015; 127:345–354.
Vessey M, Jewell D, Smith A, Yeates D, and McPherson K. Chronic inflammatory bowel disease, cigarette smoking, and use of oral contraceptives: findings in a large cohort study of women of childbearing age. British Medical Journal (Clinical Research Edition) 1986; 292:1101–1113.
ULCERATIVE COLITIS
Boyko EJ, Theis MK, Vaughan TL, and Nicol-Blades B. Increased risk of inflammatory bowel disease associated with oral contraceptive use. American Journal of Epidemiology 1994; 140:268–278.
Calkins BM, Mendeloff AI, and Garland C. Inflammatory bowel disease in oral contraceptive users. Gastroenterology 1986; 91:523–524.
Cornish JA, Tan E, Simillis C, Clark SK, Teare J, and Tekkis PP. The risk of oral contraceptives in the etiology of inflammatory bowel disease: a meta-analysis. American Journal of Gastroenterology 2008; 103:2394–2400.
Corrao G, Tragnone A, Caprilli R, Trallori G, Papi C, Andreoli A, Di Paolo M, Riegler G, Rigo GP, Ferraù O, Mansi C, Ingrosso M, and Valpiani D. Risk of inflammatory bowel disease attributable to smoking, oral contraception and breastfeeding in Italy: a nationwide case-control study. Cooperative Investigators of the Italian Group for the Study of the Colon and the Rectum (GISC). International Journal of Epidemiology 1998; 27:397–404.
García Rodríguez LA, González-Pérez A, Johansson S, and Wallander MA. Risk factors for inflammatory bowel disease in the general population. Alimentary Pharmacology & Therapeutics 2005; 22:309–315.
Godet PG, May GR, and Sutherland LR. Meta-analysis of the role of oral contraceptive agents in inflammatory bowel disease. Gut 1995; 37:668–673.
Halfvarson J, Jess T, Magnuson A, Montgomery SM, Orholm M, Tysk C, Binder V, and Järnerot G. Environmental factors in inflammatory bowel disease: a co-twin control study of a Swedish-Danish twin population. Inflammatory Bowel Disease 2006; 12:925–933.
Khalili H, Higuchi LM, Ananthakrishnan AN, Richter JM, Feskanich D, Fuchs CS, and Chan AT. Oral contraceptives, reproductive factors and risk of inflammatory bowel disease. Gut 2013; 62:1153–1159.
Lashner BA, Kane SV, and Hanauer SB. Lack of association between oral contraceptive use and ulcerative colitis. Gastroenterology 1990; 99:1032–36.
Logan RF and Kay CR. Oral contraception, smoking and inflammatory bowel disease—findings in the Royal College of General Practitioners Oral Contraception Study. International Journal of Epidemiology 1989;18:105–107.
Ng SC, Woodrow S, Patel N, Subhani J, and Harbord M. Role of genetic and environmental factors in British twins with inflammatory bowel disease. Inflammatory Bowel Disease 2012; 18:725–736.
Parrello T, Pavia M, Angelillo IF, Monteleone G, Riegler G, Papi G, D’Incà R, Annese V, Tonelli F, Caprilli R, and Pallone F. Appendectomy is an independent protective factor for ulcerative colitis: results of a multicentre case control study. The Italian Group for the Study of the Colon and Rectum (GISC). Italian Journal of Gastroenterology and Hepatology 1997; 29:208–211.
Persson PG, Leijonmarck CE, Bernell O, Hellers G, and Ahlbom A. Risk indicators for inflammatory bowel disease. International Journal of Epidemiology 1993; 22:268–272.
Sandler RS, Wurzelmann JI, and Lyles CM. Oral contraceptive use and the risk of inflammatory bowel disease. Epidemiology 1992; 3:374–378.
Vcev A, Pezerovic D, Jovanovic Z, Nakic D, Vcev I, and Majnarić L. A retrospective, case-control study on traditional environmental risk factors in inflammatory bowel disease in Vukovar-Srijem County, north-eastern Croatia, 2010. Wiener Klinische Wochenschrift 2015; 127:345–354.
Vessey M, Jewell D, Smith A, Yeates D, and McPherson K. Chronic inflammatory bowel disease, cigarette smoking, and use of oral contraceptives: findings in a large cohort study of women of childbearing age. British Medical Journal (Clinical Research Edition) 1986; 292:1101–1113.
SYSTEMIC LUPUS ERYTHEMATOSUS
Bernier MO, Mikaeloff Y, Hudson M, and Suissa S. Combined oral contraceptive use and the risk of systemic lupus erythematosus. Arthritis and Rheumatism 2009; 61:476–481.
Cooper GS, Dooley MA, Treadwell EL, St Clair EW, and Gilkeson GS. Hormonal and reproductive risk factors for development of systemic lupus erythematosus: results of a population-based, case-control study. Arthritis and Rheumatism 2002; 46:1830–1839.
Costenbader KH, Feskanich D, Stampfer MJ, and Karlson EW. Reproductive and menopausal factors and risk of systemic lupus erythematosus in women. Arthritis and Rheumatism 2007; 56:1251–1262.
Grimes DA, LeBolt SA, Grimes KR, and Wingo PA. Systemic lupus erythematosus and reproductive function: A case control study. American Journal of Obstetrics and Gynecology 1985; 153:179–186.
Sanchez-Guerrero J, Karlson EW, Liang MH, Hunter DJ, Speizer FE, and Colditz GA. Past use of oral contraceptives and the risk of developing systemic lupus erythematosus. Arthritis and Rheumatism 1997; 40: 804–808.
Strom BL, Reidenberg MM, West S, Snyder ES, Freundlich B, and Stolley PD. Shingles, allergies, family medical history, oral contraceptives, and other potential risk factors for systemic lupus erythematosus. American Journal of Epidemiology 1994; 140:632–642.
Zonana-Nacach A, Rodríguez-Guzmán LM, Jiménez-Balderas FJ, Camargo-Coronel A, Escobedo-de la Peña J, and Fraga A. [Risk factors associated with systemic lupus erythematosis in a Mexican population]. Salud Pública de México 2002; 44:213–218.
MULTIPLE SCLEROSIS
Alonso A, Jick SS, Olek MJ, Ascherio A, Jick H, and Hernán MA. Recent use of oral contraceptives and the risk of multiple sclerosis. Archives of Neurology 2005; 62:1362–1365.
Hellwig K, Chen LH, Stancyzk FZ, and Langer-Gould AM. Oral Contraceptives and Multiple Sclerosis/Clinically Isolated Syndrome Susceptibility. PLoS One 2016; 11:e0149094. Doi:10.1371/journal.pone.0149094.
Hernán MA, Hohol MJ, Olek MJ, Spiegelman D, and Ascherio A. Oral contraceptives and the incidence of multiple sclerosis. Neurology 2000; 55:848–854.
Kotzamani D, Panou T, Mastorodemos V, Tzagournissakis M, Nikolakaki H, Spanaki C, and Plaitakis A. Rising incidence of multiple sclerosis in females associated with urbanization. Neurology 2012; 78:1728–1735.
Thorogood M, and Hannaford PC. The influence of oral contraceptives on the risk of multiple sclerosis. British Journal of Obstetrics and Gynaecology 1998; 105:1296–1299.
Villard-Mackintosh L, and Vessey MP. Oral contraceptives and reproductive factors in multiple sclerosis incidence. Contraception 1993; 47:161–168.
INTERSTITIAL CYSTITIS
Champaneria R, D’Andrea RM, and Latthe PM. Hormonal contraception and pelvic floor dysfunction: a systematic review. Int Urogynecol J 2016; 27:709–722.
El Khoudary SR, Talbott EO, Bromberger JT, Chang CC, Songer TJ, and Davis EL. Severity of interstitial cystitis symptoms and quality of life in female patients. Journal of Womens Health (Larchmont) 2009; 18:1361–1368. Doi: 10.1089/jwh.2008.1270.
Gardella B, Porru D, Nappi RE, Daccò MD, Chiesa A, and Spinillo A. Interstitial cystitis is associated with vulvodynia and sexual dysfunction—a case-control study. The Journal of Sexual Medicine 2011; 8:1726–1734. Doi: 10.1111/j.1743-6109.2011.02251.x. Epub 2011 Apr 7.
Konkle K, Berry SH, Elliott MN, Hilton L, Suttorp MJ, Clauw DJ, and Clemens JQ. Comparison of an interstitial cystitis/bladder pain syndrome clinical cohort with symptomatic community women from the RAND Interstitial Cystitis Epidemiology study. Journal of Urology 2012; 187:508–512.
VENOUS THROMBOEMBOLISM
Bloemenkamp KWM, Rosendaal FR, Büller HR, Helmerhorst FM, Colly LP, and Vandenbroucke JP. Risk of venous thrombosis with use of current low-dose oral contraceptives is not explained by diagnostic suspicion and referral bias. Arch Intern Med 1999; 159:65–70.
Bloemenkamp KWM, Rosendaal FR, Helmerhorst FM, Büller HR, and Vandenbroucke JP. Enhancement by factor V Leiden mutation of risk of deep-vein thrombosis associated with oral contraceptives containing a third- generation progestagen. Lancet 1995; 346:1593–1596.
Dinger J, Assmann A, M€ohner S, and Minh TD. Risk of venous thromboembolism and the use of dienogestand drospirenone-containing oral contraceptives: results from a German case-control study. J Fam Plann Reprod Health Care 2010; 36:123–129.
Dinger J, Bardenheuer K, and Heinemann K. Cardiovascular and general safety of a 24-day regimen of drospirenonecontaining combined oral contraceptives: final results from the International Active surveillance Study of Women Taking Oral Contraceptives. Contraception 2014; 89(4):253–263.
Dinger JC, Heinemann LAJ, and Ku¨hl-Habich D. The safety of a drospirenone-containing oral contraceptive: final results from the European Active Surveillance study on oral contraceptives based on 142,475 women years of observation. Contraception 2007; 75:344–354.
Farmer RDT, Lawrenson RA, Thompson CR, Kennedy JG, and Hambleton IR. Population-based study of risk of venous thromboembolism associated with various oral contraceptives. Lancet 1997; 349:83–88.
Food and Drug Administration, Office of surveillance and epidemiology. Combined hormonal contraceptives (CHCs) and the risk of cardiovascular disease endpoints. FDA. 2011; http://www.fda.gov/downloads/Drugs/DrugSafety/UCM277384.pdf.
Gomer K. Women, Birth Control Pills, and Thrombophilia: An Analysis of Risk Communication Kerry Gomer, Clemson University. 2009; https://tigerprints.clemson.edu/cgi/viewcontent.cgi?referer=&httpsredir=1&article=1573&context=all_theses.
Gronich N, Lavi I, and Rennert G. Higher risk of venous thrombosis associated with drospirenone-containing oral contraceptives: a population-based cohort study. CMAJ 2011; 183(18):E1319-25.
Jick H, Jick SS, Gurewich V, Myers MW, and Vasilakis C. Risk of ideopathic cardiovascular death and nonfatal venous thromboembolism in women using oral contraceptives with differing progestagen components. Lancet 1995; 346:1589-1593.
Jick SS, and Hernandez RK. Risk of non-fatal venous thromboembolism in women using oral contraceptives containing drospirenone compared with women using oral contraceptives containing levonorgestrel: case-control study using United States claims data. British Medical Journal 2011; 340:d2151.
Keenan L, Kerr T, Duane M, and Van Gundy K. Systematic Review of Hormonal Contraception and Risk of Venous Thrombosis. The Linacre Quarterly 2018; 85(4):470–477.
Le Moigne E, Delluc A, Tromeur C, Nowak E, Mottier D, Lacut K, and Le Gal G. Risk of recurrent venous thromboembolism among young women after a first event while exposed to combined oral contraception versus not exposed to: a cohort study. Thromb Res 2013; 132:51–55.
Lewis MA, MacRae KD, Kűhl-Habich D, Bruppacher R, Heinemann LA, and Spitzer WO. The differential risk of oral contraceptives: the impact of full exposure history. Hum Re prod 1999; 14:1493–1499.
Lidegaard Ø, Edstr€om B, and Kreiner S. Oral contraceptives and venous thromboembolism. A five-year national case-control study. Contraception 2002; 65:187–196.
Lidegaard Ø, Løkkegaard E, Svendsen AL, and Agger C. Hormonal contraception and risk of venous thromboembolism: national follow-up study. British Medical Journal 2009; 339:b2890.
Lidegaard Ø, Nielsen LH, Skovlund CW, and Løkkegaard E. Venous thrombosis in users of non-oral hormonal contraception: follow-up study, Denmark 2001–10. British Medical Journal 2012; 344:e2990.
Lidegaard Ø,Nielsen LH, Skovlund CW, Skjeldestad FE, and Løkkegaard E. Risk of venous thromboembolism from use of oral contraceptives containing different progestogens and estrogen doses: Danish cohort study 2001–2009. British Medical Journal 2011; 343:d6423.
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Parkin L, Skegg DCG, Wilson M, Herbison GP, and Paul C. Oral contraceptives and fatal pulmonary embolism. Lancet 2000; 355:2133–2134.
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Spitzer WO, Lewis MA, Heinemann LAJ, Thorogood M, and MacRae KD. Third generation oral contraceptives and risk of venous thromboembolic disorders: an international case-control study. British Medical Journal 1996; 312:83-88.
Todd J-C, Lawrenson R, Farmer RDT, Williams TJ, and Leydon GM. Venous thromboembolic disease and combined oral contraceptives: a re-analysis of the MediPlus database. Hum Reprod 1999; 14:1500–1505.
Van Hylckama VA, Helmerhorst FM, Vandenbroucke JP, Doggen CJ, and Rosendaal FR. The Venous Thrombotic Risk of Oral Contraceptives, Effects of Estrogen Dose and Progestogen Type: Results of the MEGA Case-Control Study. British Medical Journal 2009; 339:b2921. Doi:10.1136/bmj.b2921.
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ATHEROSCLEROSIS AND CARDIOVASCULAR EVENTS
Bagdade JD and Subbaiah PV. Serum from Oral Contraceptive Users Stimulates Growth of Arterial Smooth Muscle Cells. AHA Journals, Arteriosclerosis 1982; 2(2):170–176.
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Hickson SS, Miles KL, McDonnell BJ, Yasmin, Cockcroft JR, Wilkinson IB, McEniery CM; ENIGMA Study Investigators. Use of the oral contraceptive pill is associated with increased large artery stiffness in young women: the ENIGMA study. J Hypertens 2011; 29(6):1155–1159.
Heidarzadeh Z, Asadi B, Saadatnia M, Ghorbani A, and Fatehi F. The Effect of Low-dose Combined Oral Contraceptive Pills on Brachial Artery Endothelial Function and Common Carotid Artery Intima–Media Thickness. Journal of Stroke and Cerebrovascular Diseases 2014; 23:675–680.
Lidegaard Ø, Løkkegaard E, Jensen A, Skovlund CW, and Keiding N. Thrombotic stroke and myocardial infarction with hormonal contraception. N Engl J Med 2012; 366:2257–2266.
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BREAST CANCER
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Alipour S, Omranipour R, Malekzadeh R, Poustchi H, Pourshams A, Khoshnia M, Gharavi A, Roshandel G, Eslami B. A Case-Control Study of Breast Cancer in Northeast of Iran: The Golestan Cohort Study. Arch Iran Med. 2019 Jul 1;22(7):355-360.
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Amadou A, Fabre A, Torres-Mejía G, Ortega-Olvera C, Angeles-Llerenas A, McKenzie F, Biessy C, Hainaut P, and Romieu I. Hormonal therapy and risk of breast cancer in Mexican women. PLoS One 2013; 8:e79695.
Barańska A, Kanadys W. Oral Contraceptive Use and Breast Cancer Risk for BRCA1 and BRCA2 Mutation Carriers: Systematic Review and Meta-Analysis of Case-Control Studies. Cancers (Basel). 2022 Sep 29;14(19):4774.
Beaber EF, Buist DS, Barlow WE, Malone KE, Reed SD, and Li CI. Recent oral contraceptive use by formulation and breast cancer risk among women 20 to 49 years of age. Cancer Res 2014a; 74:4078–4089.
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