Abortifacient Agents: Chemical substances that interrupt pregnancy after implantation.Pinus ponderosa: A plant species of the genus PINUS that contains isocupressic acid.Abortifacient Agents, Nonsteroidal: Non-steroidal chemical compounds with abortifacient activity.Abortifacient Agents, Steroidal: Steroidal compounds with abortifacient activity.Trichosanthin: Plant-derived ribosome-inactivating protein (RIP) purified from the Chinese medicinal herb tian-hua-fen which is obtained from the root tubers of Trichosanthes kirilowii. It has been used as an abortifacient and in the treatment of trophoblastic tumors. GLQ223 (Compound Q), a highly purified form of trichosanthin, has been proposed as antiviral treatment for AIDS.Abortion, Veterinary: Premature expulsion of the FETUS in animals.Abortion, Induced: Intentional removal of a fetus from the uterus by any of a number of techniques. (POPLINE, 1978)Anti-Inflammatory Agents, Non-Steroidal: Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.Pregnancy: The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH.

Effect of DL111-IT on progesterone biosynthesis and viability of rat luteal cells in vitro. (1/197)

AIM: To study the influence of DL111-IT on progesterone biosynthesis of cultured luteal cells (LC). METHODS: LC viability was assessed with trypan blue dye exclusion and progesterone concentration was measured with radioimmunoassay. RESULTS: DL111-IT decreased the viability of LC after 24-h incubation, its ED50 being 7.7 (95% confidence limits: 7.1-8.5) mg.L-1. DL111-IT inhibited basal secretion of progesterone in a concentration-dependent manner, and 3 mg.L-1 decreased progesterone concentration by 25% vs control. DL111-IT 3 mg.L-1 also inhibited the stimulatory effect of forskolin (cAMP activator) 10 mumol.L-1 and pregnenolone [converted to progesterone by 3 beta-hydroxysteroid dehydrogenase-isomerase complex (3 beta-HSD)] 10 mumol.L-1 on progesterone production in cultured LC, and their inhibitory rates were 43% and 155%, respectively. At the same concentration, DL111-IT did not influence hCG-induced progesterone production. CONCLUSION: DL111-IT inhibited progesterone synthesis by suppressing the conversion of pregnenolone to progesterone (inactivating 3 beta-HSD) and suppressed the activity of cAMP. DL111-IT 6-24 mg.L-1 decreased the viability of LC.  (+info)

The effectiveness of non-surgical management of early interstitial pregnancy: a report of ten cases and review of the literature. (2/197)

OBJECTIVE: To assess the effectiveness of non-surgical management of interstitial pregnancy. DESIGN: A prospective interventional study. SUBJECTS: Eleven women with the ultrasound diagnosis of interstitial ectopic pregnancy. METHODS: Women with suspected early pregnancy complications were examined by transvaginal ultrasound. Those with the diagnosis of interstitial pregnancy were offered non-surgical treatment with methotrexate, which was administered systemically or by local injection. Follow-up with regular measurements of beta-human chorionic gonadotropin and ultrasound scans continued until the pregnancy had resolved completely. RESULTS: Ten women were managed non-surgically, and one woman opted for surgery. Five women received systemic and five local methotrexate. Local therapy was successful in all five cases (100%), whereas four out of five (80%) women receiving systemic methotrexate were cured. Significant side-effects were noted in two women following systemic therapy. In comparison, there were no side-effects in the group of women who received local therapy. There were no significant differences between the two treatment groups in the length of time taken for the pregnancy to resolve. CONCLUSIONS: Non-surgical treatment of interstitial pregnancy with methotrexate appears to be safe and effective. Local administration appears to be more successful and better tolerated by patients and may be used as the first-line therapy.  (+info)

Once-a-month treatment with a combination of mifepristone and the prostaglandin analogue misoprostol. (3/197)

In this two centre study, the efficacy of 200 mg mifepristone orally followed 48 h later by 0.4 mg misoprostol orally for menstrual regulation was investigated. The dose of mifepristone was taken the day before the expected day of menstruation. Each volunteer was planned to participate for up to 6 months. A plasma beta human chorionic gonadotrophin (HCG) was measured on the day of mifepristone intake. The study was disrupted prematurely due to low efficacy. In 125 treatment cycles the overall pregnancy rate was 17.6% (22 pregnancies) and the rate of continuing pregnancies (failure) was 4.0%. Eight women discontinued the study due to bleeding irregularities which were seen in 15 cycles (12%). These effects on bleeding pattern made the timing of treatment day difficult. Late luteal phase treatment with a combination of mifepristone and misoprostol is not adequately effective for menstrual regulation.  (+info)

Angiotensin II interacts with prostaglandin F2alpha and endothelin-1 as a local luteolytic factor in the bovine corpus luteum in vitro. (4/197)

Recent findings suggest that the ovarian renin-angiotensin system may regulate ovarian function through the paracrine/autocrine actions of angiotensin II (Ang II). In this study, we have examined and characterized the local effects of Ang II as a luteolytic factor and its interaction with prostaglandin F2alpha (PGF2alpha) and endothelin-1 (ET-1) in the bovine corpus luteum (CL) of the mid-luteal phase, by using an in vitro microdialysis system (MDS). Ang II was detected in the MDS perfusate (4 pg/ml), and infusion of PGF2alpha (10(-6) M) for 2 h increased the Ang II release by 50-100% during the following experimental period, in addition to its stimulation of ET-1 release. Two 2-h infusions of Ang II (10(-7)-10(-5) M) separated by a 2-h interval induced a dose- and time-dependent decrease of progesterone (P4) release by 41-66%. When the luteal explants were pre-perfused with PGF2alpha (10(-6) M) for 2 h, two consecutive perfusions of Ang II (10(-6) M) at a 2-h interval rapidly reduced the P4 release (by 50%). This reduction occurred 6 h earlier than those of infusions of PGF2alpha or Ang II alone. The simultaneous infusion of either 1) Ang II (10(-6) M) with PGF2alpha (10(-6) M), 2) ET-1 (10(-7) M) with PGF2alpha, or 3) Ang II + ET-1 with PGF2alpha (10(-6) M) for 2 h also induced a rapid and pronounced (60%) decrease in P4 release. Perfusion with the Ang II antagonist blocked the P4-suppressing activity of Ang II alone or PGF2alpha + Ang II infusion. Ang II stimulated the release of ET-1 and oxytocin during infusion but inhibited them after infusion. These results show that Ang II is released in the bovine midcycle CL in vitro, and this peptide, either alone or together with PGF2alpha, can suppress the release of P4. As PGF2alpha directly stimulated Ang II release, Ang II may influence the critical period for starting the cascade of functional luteolysis in vivo and might lead to structural luteolysis with ET-1 as a major vasoconstrictor. The overall results suggest that Ang II may have an important role at luteolysis in the bovine CL.  (+info)

Does an acidic medium enhance the efficacy of vaginal misoprostol for pre-abortion cervical priming? (5/197)

Absorption pharmacokinetics reveal a relationship between plasma concentrations of misoprostol and its therapeutic effect. To achieve a constant plasma profile and optimal efficacy, it is important to develop a medium that ensures complete dissolution of vaginal misoprostol tablets. Vaginal misoprostol is said to liquefy better in an acidic medium; thus, the aim of this study was to determine whether a 200 microg misoprostol tablet dissolved in acetic acid would be more efficacious than 200 microg misoprostol dissolved in water for pre-abortion cervical priming. A total of 120 healthy nulliparous women requesting legal termination of pregnancy between 6-12 weeks gestation were allocated randomly to either of the study groups. Vacuum aspiration was performed 3-4 h after insertion of the misoprostol tablet. Using Hegar's dilator, the degree of cervical dilatation before operation was measured. Of 60 women, 14 (23%) achieved a cervical dilatation of >/=8 mm when the misoprostol dose was dissolved in acetic acid; 12 (20%) achieved a similar cervical dilatation when the dose was dissolved in water. The mean cervical dilatation for the acid and water media used was 6.3 mm and 6.2 mm respectively; these differences were not statistically significant, neither were pre-operative and intra-operative blood losses statistically different between the two groups. Twenty-four (40%) and four (7%) respectively of women in whom a water medium was used experienced vaginal bleeding and abdominal pain; 20 (33%) and 0 women respectively among those in whom an acetic acid medium was used experienced vaginal bleeding and abdominal pain. These differences in side effects were not statistically significant. Our study shows that the use of acetic acid to dissolve vaginal misoprostol does not improve the efficacy in achieving successful cervical dilatation for pre-abortion cervical priming.  (+info)

The use of misoprostol for pre-operative cervical dilatation prior to vacuum aspiration: a randomized trial. (6/197)

Misoprostol is effective for cervical priming prior to vacuum aspiration for first trimester termination of pregnancy. Previous studies showed that the oral route was more acceptable to patients but there were higher incidences of side-effects when compared with the vaginal route. This study is to determine the optimal dosage and route of administration of misoprostol for pre-operative cervical dilatation. A double-blind, randomized trial was undertaken for 225 nulliparous women with 8-12 weeks amenorrhoea. They were randomly assigned to groups given 0 (placebo), 200 or 400 microg oral or vaginal misoprostol 3 h prior to vacuum aspiration. In misoprostol-treated groups the baseline cervical dilatation was significantly increased when compared with the placebo group; the effect was dose-related in the oral but not in the vaginal group. The cumulative force and blood loss was significantly decreased in the misoprostol-treated groups. The incidences of side-effects were more frequent in misoprostol groups but were not related to the route and dosage of medication. The duration of procedure, incidences of post-operative complications, the duration of post-operative bleeding and the interval to the first period were similar in the five treatment groups. We conclude that a 3 h pre-treatment interval is effective for both oral and vaginal routes. When given orally, 400 microg is more effective than 200 microg. The efficacy was otherwise similar when compared with the vaginal route. We recommend 400 microg oral misoprostol 3 h prior to vacuum aspiration for cervical dilatation.  (+info)

Induction of parturition in bitches with minimal side effects by two injections of a low dose of fenprostalene, a prostaglandin F2alpha analogue, and pretreatment with prifinium bromide. (7/197)

An experiment using 16 Beagle bitches (aged 11 months to 6 years and 2 months) in their 56th to 58th day of pregnancy was carried out to investigate the effects of two injections of a low dose of fenprostalene, a long-acting prostaglandin F2alpha analogue, and pretreatment with prifinium bromide, a parasympathetic nerve blocking agent, on the induction of parturition and severity of side effects. The bitches were divided into three treatment groups: one injection of 5 microg/kg of fenprostalene (group I, n=5); one injection of 7.5 mg/head of prifinium bromide followed by one injection of 5 microg/kg of fenprostalene at 5 min after prifinium bromide injection (group II, n=6); and one injection of 7.5 mg/head of prifinium bromide followed by two injections of 2.5 microg/kg of fenprostalene, one injection at 5 min after prifinium bromide injection and the next at 1 hr after the fenprostalene first injection (group III, n=5). Following the injection of fenprostalene, side effects such as salivation, vomiting, colic symptoms, and watery diarrhea occurred most frequently (80-100% of cases) in group I bitches. Apart from colic symptoms, no side effects were observed in group III bitches. Group III bitches also showed the smallest increase in plasma cortisol concentration. No significant difference in the time to initiation of parturition was found between the three groups. The one-week survival rate of newborn puppies was highest in group III. The results showed that pretreatment with prifinium bromide and two injections of 2.5 microg/kg of fenprostalene can alleviate side effects following fenprostalene administration and have no adverse effect on the survival of newborn puppies, indicating that this method is a reliable and safe way of inducing parturition in bitches.  (+info)

A comparison of two regimens of intravaginal misoprostol for termination of second trimester pregnancy: a randomized comparative trial. (8/197)

A prospective randomized trial was conducted in 148 women to compare the efficacy of two regimens of vaginal misoprostol for termination of second trimester pregnancy. Women aged 16-40 years requesting termination of second trimester pregnancy were randomized into two groups. Women in group 1 were given vaginal misoprostol 400 microg every 3 h for a maximum of five doses in 24 h. Women in group 2 were given vaginal misoprostol 400 microg every 6 h for a maximum of three doses in 24 h. If women did not abort in 24 h, the same regimen was repeated. The median induction-abortion interval in group 1 (15.2 h) was significantly shorter (P < 0.01) than that in the group 2 (19.0 h). The percentage of women who achieved successful abortion within 48 h in group 1 (90.5%) was also significantly higher (P < 0.02) than that in group 2 (75.7%). The incidence of fever was more common in group 1 (P = 0.01). It is concluded that the regimen of vaginal misoprostol 400 microg every 3 h with maximum of five doses in 24 h was more effective than the regimen of misoprostol every 6 h in termination of second trimester pregnancy.  (+info)

*List of MeSH codes (D16)

... abortifacient agents MeSH D27.505.696.875.131.100 --- abortifacient agents, nonsteroidal MeSH D27.505.696.875.131.200 --- ... abortifacient agents MeSH D27.505.954.705.131.100 --- abortifacient agents, nonsteroidal MeSH D27.505.954.705.131.200 --- ... anti-inflammatory agents MeSH D27.505.954.158.030 --- anti-inflammatory agents, non-steroidal MeSH D27.505.954.158.030.500 --- ... antirheumatic agents MeSH D27.505.954.329.030 --- anti-inflammatory agents, non-steroidal MeSH D27.505.954.329.337 --- gout ...

*Methotrexate

... is an abortifacient and is commonly used to terminate pregnancies during the early stages, generally in ... Recently, use of methotrexate in combination with anti-TNF agents has been shown to be effective for the treatment of ... Colebatch, AN (2011). "Safety of non-steroidal anti-inflammatory drugs, including aspirin and paracetamol (acetaminophen) in ... Methotrexate (MTX), formerly known as amethopterin, is a chemotherapy agent and immune system suppressant. It is used to treat ...
The main purpose of our study was to which determine factors, those measured by ultrasound and also demographic and clinical factors (age, number of previous pregnancies, abortions and deliveries) predict outcome of medical treatment for early pregnancy failure. Our hypothesis was that gestational sac volume predicts outcome of medical treatment for early pregnancy failure ...
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies. ...
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Results: The success rate is greater in mifepristone with misoprostol group with 98% than misoprostol group with 90% Mean induction abortion interval from the insertion of the first misoprostol tablet is significantly shorter in the mifepristone pretreated group 12.93+4.19 hr as compared to 19.18+3.97 hr in the misoprostol alone group (p,0.001). The mean dose of the misoprostol required is significantly less in the mifepristone group as against misoprostol group (p=0.008). The side effects and complications observed in both the groups are mainly nausea vomiting, fever, abdominal cramps, bleeding, rigor, dizziness, retained products of consumption and these side effects are more in misoprostol group ...
OBJECTIVE To compare the efficacy of 400 microg of misoprostol with that of 1 mg of gemeprost as cervical priming agents when administered vaginally 3 to 4 hours before first-trimester vacuum aspiration abortion. METHODS In a prospective controlled trial 90 nulliparous women who requested termination of pregnancy before 12 weeks gestation were randomized to receive vaginally either misoprostol or gemeprost for cervical priming. The force to dilate the cervix was measured by the use of a cervical tonometer connected to Hegar dilators from 3 to 10 mm. The main outcome measures were baseline cervical dilation; the peak force to dilate the cervix at 8, 9, and 10 mm; and the cumulative force to dilate the cervix to 10 mm. RESULTS Baseline cervical dilation did not differ significantly between the women who received misoprostol and those who were treated with gemeprost. Neither the peak force required to dilate the cervix at 8, 9, and 10 mm nor the cumulative force to dilate the cervix to 10 mm showed
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A Cervical pregnancy is an ectopic pregnancy that has implanted in the uterine endocervix. Such a pregnancy typically aborts within the first trimester, however, if it is implanted closer to the uterine cavity - a so-called cervico-isthmic pregnancy - it may continue longer. Placental removal in a cervical pregnancy may result in major hemorrhage. The incidence has been reported to be about 1:1,000 to 1: 16,000 pregnancies. Pregnancies involving the isthmus - the segment of the uterus between the cervix and the fundus - are more common than true cervical pregnancies. While in many situations the cause of the abnormal implantation remains unclear, there is evidence to link the development of cervical pregnancy to uterine instrumentation, specifically repeated D&Cs (dilatation and curettage). Cervical pregnancies are to be distinguished from pregnancies that start from an implantation in a scar of a previous cesarean section, so-called scar pregnancies. The diagnosis is made in asymptomatic ...
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BACKGROUND: This study was conducted to evaluate the efficacy and side effects of a new regimen of 800 microg misoprostol administered intravaginally every 6 h up to a maximum of three doses in 24 h for second trimester pregnancy termination. METHODS
Th is study will compare sequential mifepristone and misoprostol (M&M) treatment versus misoprostol treatment alone, which is currently the standard medical
Human Reproduction. Advance Access, May 5, 2005, pp 1-7.. 55. Hedley, Ellertson, Trussell ed, Accounting for time: Insights from a life-table analysis of the efficacy of medical abortion. American Journal of Obstetrics and Gyneacology (2004) 191, pp 1928-33. 56. Timothy Craig, Cathy Mende. Common allergic and allergic-like reactions to medications. Postgraduate Medicine, vol105/ no 3/ March 1999. 57. Prof P Potter, Allergy society of South Africa Retrieved August 12, 2005. 58. G William Palmer, Stephen Dreskin, Anaphylaxis. E-Medicine, October 2004. pp 3. Retrieved August 12, 2005. 59. Hamoda, Ashok, Flett, Templeton, A randomized controlled trial of Mifepristone in combination with misoprostol administered sublingually or vaginally for medical abortion up to 13 weeks of gestation. BJOG 2005 Aug; 112(8): 1102-8. 60. CBC trust. 61. Middleton T, Schaff EA, Fielding SL, Scahill M, Shannon C, Westheimer E, Wilkinson T, Winikoff B. Randomized trial of mifepristone and buccal or vaginal misoprostol ...
Use misoprostol as directed by your doctor. Check the label on the medicine for exact dosing instructions. An extra patient leaflet is available with misoprostol. Talk to your pharmacist if you have questions about this information. Take misoprostol by mouth with food unless your doctor tells you otherwise. The last dose of the day should be taken at bedtime. Taking misoprostol after meals and at bedtime may decrease the risk of diarrhea. Do not take an antacid that has magnesium in it within 1 hour before or 2 hours after you take misoprostol. If you miss a dose of misoprostol, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Ask your health care provider any questions you may have about how to use misoprostol ...
Use misoprostol as directed by your doctor. Check the label on the medicine for exact dosing instructions. An extra patient leaflet is available with misoprostol. Talk to your pharmacist if you have questions about this information. Take misoprostol by mouth with food unless your doctor tells you otherwise. The last dose of the day should be taken at bedtime. Taking misoprostol after meals and at bedtime may decrease the risk of diarrhea. Do not take an antacid that has magnesium in it within 1 hour before or 2 hours after you take misoprostol. If you miss a dose of misoprostol, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Ask your health care provider any questions you may have about how to use misoprostol ...
Use misoprostol as directed by your doctor. Check the label on the medicine for exact dosing instructions. An extra patient leaflet is available with misoprostol. Talk to your pharmacist if you have questions about this information. Take misoprostol by mouth with food unless your doctor tells you otherwise. The last dose of the day should be taken at bedtime. Taking misoprostol after meals and at bedtime may decrease the risk of diarrhea. Do not take an antacid that has magnesium in it within 1 hour before or 2 hours after you take misoprostol. If you miss a dose of misoprostol, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Ask your health care provider any questions you may have about how to use misoprostol ...
Use misoprostol as directed by your doctor. Check the label on the medicine for exact dosing instructions. An extra patient leaflet is available with misoprostol. Talk to your pharmacist if you have questions about this information. Take misoprostol by mouth with food unless your doctor tells you otherwise. The last dose of the day should be taken at bedtime. Taking misoprostol after meals and at bedtime may decrease the risk of diarrhea. Do not take an antacid that has magnesium in it within 1 hour before or 2 hours after you take misoprostol. If you miss a dose of misoprostol, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Ask your health care provider any questions you may have about how to use misoprostol ...
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The widespread use of NSAIDs has led to increased recognition of their adverse effects on the upper gastrointestinal tract. NSAIDs cause dyspepsia in many patients, and a small number develop clinically significant ulcers and complications. The prevention of adverse events from NSAIDs includes the use of low-risk agents and co-prescription with prostaglandins or acid inhibitors (1). The meta-analysis by Koch and colleagues examines the ability of H2 blockers and misoprostol to reduce NSAID-induced mucosal injury that was measured by endoscopy. This type of injury, which has uncertain clinical importance, was used as an outcome measure instead of more relevant outcomes, such as reduction in serious ulcer complications. As shown by this meta-analysis, misoprostol reduces both gastric and duodenal ulcers. More important, although misoprostol has been shown to reduce serious adverse events, the NNT is 264 to prevent a single complication (2). This leads us to consider whether misoprostol is ...
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An abnormally low sac position can result from several possibilities which include impending / ongoing miscarriage cervical ectopic pregnancy fundal fibroid or other mass compressing the sac downward
The debate in the House has begun on whether to require most women to receive and pay for an ultrasound before having an abortion. As the questions began getting into the details (vaginal ultrasounds, fallopian tubes, fetuses, etc.) of various...
Misoprostol abortion inducing drug molecule. Prostaglandin E1 (PGE1) analogue also used to treat missed miscarriage, induce labor, etc. Stylized skeletal formula (chemical structure). Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey), oxygen (red). - Stock Image F013/0558
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Misoprostol CAS:59122-46-2 Molecular Formula: C22H38O5 Molecular Weight: 382.60 Chemical Properties: White Solid Assay:99% Solubility: Soluble to 100 mM in Ethanol Safety: Poison by ingestion, intramuscular, and intraperitoneal routes. When heated...
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The information presented at the site has a general character. Note please this information cannot be used for self-treatment and self diagnosis. You should consult with your doctor or health care adviser regarding any specific instructions of your condition. The information is reliable, but we concede it could contain mistakes. We are not responsible for any direct, indirect, special or other damage caused by use of this information on the site and also for consequences of self-treatment ...
The information presented at the site has a general character. Note please this information cannot be used for self-treatment and self diagnosis. You should consult with your doctor or health care adviser regarding any specific instructions of your condition. The information is reliable, but we concede it could contain mistakes. We are not responsible for any direct, indirect, special or other damage caused by use of this information on the site and also for consequences of self-treatment ...
The information presented at the site has a general character. Note please this information cannot be used for self-treatment and self diagnosis. You should consult with your doctor or health care adviser regarding any specific instructions of your condition. The information is reliable, but we concede it could contain mistakes. We are not responsible for any direct, indirect, special or other damage caused by use of this information on the site and also for consequences of self-treatment ...
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ive asked a question here about if it was possible to still be pregnant after taking misoprostol and i was told it was i wasalso adviced to either keep the pregnancy or go for a d&c, i went for a d&c
At least Once a week, I read something for class and realize that i already know it because of SVU! Anyone else notice this? Example: Misoprostol should not be used in women who are pregnant or
Product Name: Mifepristone and Misoprostol Tablets. Common Name: contraceptive pills. Strength: available in -. Mifepristone IP 200mg & Misoprostol IP 200mcg. Description: Medical Abortion is a form of early abortion caused by the combination of two medications, mifepristone and misoprostol that is an option for women who are 8 weeks pregnant or less. Also known as RU486 or medication abortion.. During the first appointment at the clinic you receive the mifepristone pill to take orally. Then 24 to 72 hours later, in the privacy, take the the second medication, misoprostol. Misoprostol causes contractions resulting in a miscarriage. When used in combination, mifepristone and misoprostol are 95-97% effective within two weeks. Mifepristone and misoprostol are FDA approved.. Indications and Usage: Mifepristone is used in combination with misoprostol (Cytotec) to end an early pregnancy. Early pregnancy means it has been 70 days or less since your last menstrual period began. Mifepristone is in a ...
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This study sought to assess the feasibility and acceptability of introducing medical abortion up to 63 days LMP in Uzbekistan, with the option of home administration of misoprostol. Findings include a high success rate and high acceptability among participants. In addition, almost all women chose to administer the misoprostol at home.. Access the abstract.. ...
Usually women do not feel anything after taking the mifepristone (the first pill that is swallowed). A few women have reported experiencing some nausea, dizziness, or very light bleeding.. After taking misoprostol, you may initially feel side effects from the misoprostol, including a light fever, chills, diarrhea, and nausea. These are normal side effects and usually pass within a few hours or so of using the misoprostol.. The misoprostol will cause cramping and bleeding as the uterus contracts and pushes out the pregnancy. If a woman uses mifepristone plus misoprostol, the cramps and bleeding usually start within 1-5 hours after using the misoprostol, but some women have cramps sooner and some later; every womans body is different. If a woman is using misoprostol alone, most women will start bleeding within 7 hours after using misoprostol; however it may start several hours sooner or later. It can be different in every case.. Bleeding is usually heavier than a period and often accompanied by ...
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Induced Abortion." The American College of Obstetricians and Gynecologists. 2001.. Pymar HC, Creinin MD (2000). Alternatives to mifepristone regimens for medical abortion. American Journal of Obstetrics and Gynecology, 183 (2): s54-s64.. Paul M, et al. (1999). A Clinicians Guide to Medical and Surgical Abortion. New York: Churchill Livingstone.. Creinin MD, et al. (2001). Medical management of abortion. American Journal of Obstetrics and Gynecology Practice Bulletin, no. 26, pg.1-13.. Goldberg ab, et al. (2001). Misoprostol and pregnancy. New England Journal of Medicine, 344 (1): 3845.. Spitz IM, et al. (1998). Early pregnancy termination with mifepristone and misoprostol in the U.S. New England Journal of Medicine, 338 (18): 1241-1247.. ...
An observational study including 276 patients with early pregnancy failure was performed to evaluate the clinical and ultrasound factors influencing the efficacy of misoprostol in the treatment of first trimester pregnancy failure. Gestational age di
Looking for incomplete abortion? Find out information about incomplete abortion. Expulsion of only part of the product of conception, with some of the membranes or placenta remaining in the uterus Explanation of incomplete abortion
An interstitial pregnancy is a uterine but ectopic pregnancy; the pregnancy is located outside the uterine cavity in that part of the fallopian tube that penetrates the muscular layer of the uterus. The term cornual pregnancy is sometimes used as a synonym, but remains ambiguous as it is also applied to indicate the presence of a pregnancy located within the cavity in one of the two upper "horns" of a bicornuate uterus. Interstitial pregnancies have a higher mortality than ectopics in general. The part of the Fallopian tube that is located in the uterine wall and connects the remainder of the tube to the endometrial cavity is called its "interstitial" part, hence the term "interstitial pregnancy"; it has a length of 1-2 cm and a width of 0.7 cm. Its borders are the opening (ostium) of the tube to the endometrial cavity within the uterus and, laterally, the visible narrow segment of the tube. The area is well supplied by the Sampson artery which is connected to both the uterine and the ovarian ...
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The efficacy of 400 micrograms misoprostol daily in the prevention of NSAID (non-steroidal anti-inflammatory drug)-induced gastric ulcer has been proven. We calculated the cost-effectiveness of a 3-month course of treatment of 200 micrograms twice daily for patients of the sick fund Wiener Gebietskrankenkasse, based on charges of the year 1993. Since efficacy in preventing NSAID-induced gastric ulcers has not yet been proven for any other drug, we compared misoprostol-treated patients with untreated controls. The model was based on the following assumptions: 70% compliance with respect to misoprostol treatment, 5.6% incidence of gastric ulcer in patients protected with misoprostol, 21.7% incidence among unprotected NSAID users, 20% hospitalisation among patients with gastric ulcer. When using Kassenpreis (drug price paid by the sick funds) misoprostol treatment is cost-effective at costs of AS 64,100,--for inpatient care, upwards and at costs of AS 43,361,-upwards when using Apothekeneinstandspreis
Induced Abortion. The American College of Obstetricians and Gynecologists. 2001.. Pymar HC, Creinin MD (2000). Alternatives to mifepristone regimens for medical abortion. American Journal of Obstetrics and Gynecology, 183 (2): s54-s64.. Paul M, et al. (1999). A Clinicians Guide to Medical and Surgical Abortion. New York: Churchill Livingstone.. Creinin MD, et al. (2001). Medical management of abortion. American Journal of Obstetrics and Gynecology Practice Bulletin, no. 26, pg.1-13.. Goldberg ab, et al. (2001). Misoprostol and pregnancy. New England Journal of Medicine, 344 (1): 3845.. Stewart GK (1998). Intrauterine devices. In RA Hatcher et al., eds., Contraceptive Technology, 17th rev.ed., pp.511-544. New York: Ardent Media.. Spitz IM, et al. (1998). Early pregnancy termination with mifepristone and misoprostol in the U.S. New England Journal of Medicine, 338 (18): 1241-1247.. ...
Medical extinction of maternity widely exerts at early stage of 1st trimester of pregnancy including mifepristone in grouping with a prostaglandin analog range to 7 weeks of supposition length. Moreover, the grouping of Mifepristone & misoprostol equally works fabulous & responsive to abandon an early pregnancy. Generally, the path of pregnancy termination includes 7 weeks of incubation; therapeutic extinction using mifepristone-misoprostol calculated wide working than vacuum aspiration. This consequences when the clinically work out fail to engross any wide scrutiny of expressed tissue. One after practice of mifepristone must take misoprostol with the gap of 24-48 hours late than buccal or vaginal misoprostol is prescribed to exercise to get 98% active response of ending early pregnancy. One needs to exercise mifepristone & misoprostol to end early pregnancy not for the late pregnancy. One must maintain the pregnancy of 7 to 8 weeks of duration to include in medical abortion process as moving ...
Results 748 women were randomised to either 600 µg misoprostol (n = 374) or placebo (n = 374). 93% of women were followed up and 80% of drug packets (both used and unused) were retrieved. 56.7% of women took the study medication. Medication was taken before delivery in 2 women (both in the misoprostol group) and no harm was reported. The primary outcome (fall in Hb ,20%) occurred in 7.3% of recruits. There were no significant differences between the groups in the rate of postnatal anaemia or self-reported blood loss. There was significantly more self-reported fever and shivering in the misoprostol group but acceptability of side effects was high.. ...
The United Kingdoms largest independent abortion provider is mounting a High Court challenge to make it possible for women to complete early stage abortions at home.. BPAS, formerly known as the British Pregnancy Advisory Service, is asking the court to rule that the 1967 Abortion Act allows women to take the second dose of tablets for an early medical abortion at home.. The act says that any treatment for the termination of pregnancy has to be carried out at a hospital or clinic. Early medical abortion, available in the first nine weeks of … ...
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MTP Kit (combination of Mifepristone and Misoprostol tablet) is quite effective in the termination of an early pregnancy of 9 weeks of gestation. MTP Kit encloses two important FDA-approved medicines called Mifepristone and Misoprostol. Abortion kit Mifepristone and Misoprostol online USA fast delivery. Know more from here @ PillsUneed.com
As ladies, we know pregnancy happens. And, sometimes pregnancies dont go as planned.. Labor can be difficult. Postpartum bleeding can happen: postpartum hemorrhage (PPH) is the number one cause of maternal mortality in many African countries. Also, we can lose the baby through a miscarriage or spontaneous abortion. Or, we may terminate the pregnancy - have an abortion - for many reasons.. Many things can happen when youre pregnant. But, medical advances - especially affordable ones that can be used in low-income settings - havent been common.. Enter misoprostol. Misoprostol was developed in the 1980s as a stomach ulcer drug and was not prescribed for pregnant women because it could cause miscarriage. As medical providers began to understand the effect misoprostol had on the cervix and uterus, they began to use it "off label" to induce labor, medically manage miscarriages and for medical abortion.. Many African countries are leading the way in registering misprostol officially for obygn and ...
Molecular research shows misoprostol prevents cell communication.. A York University study has shown for the first time how the drug misoprostol, which has been linked to neurodevelopmental defects associated with autism, interferes with neuronal cell function.. It is an important finding because misoprostol is similar in structure to naturally-occurring prostaglandins, which are the key signaling molecules produced by fatty acids in the brain.. Past clinical studies have shown an association between misoprostol and severe neurodevelopmental defects including autism symptoms. Those studies looked at cases in Brazil in which women misused the drug early in pregnancy in unsuccessful attempts to terminate their pregnancies.. The York study examined mouse neuronal cells to discover how the drug actually interferes at a molecular level with prostaglandins, which are important for development and communication of cells in the brain.. "Early in the first trimester of pregnancy, neuronal cells reach out ...
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More scientific information:. Research has shown that for women with pregnancies of 8 weeks or less, Misoprostol works with the same efficacy whether it is taken at 12 hours, 24 hours, 48 hours, or as much as 72 hours after Mifepristone.7 Though we instruct women to take Misoprostol 24 hours after Mifepristone and strongly encourage women to follow all the instructions for proper use, if a woman takes it slightly earlier or later, this does not effect the outcome of the medical abortion. 102 ...
Le misoprostol est plus efficace que la sonde de Foley pour déclencher le travail sur un col non favorable. Le fait que cela augmente lincidence des hypertonies ne semble pas affecter les auteurs.
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Cette note dinformation stratégique, publié par la FCI en partenariat avec Gynuity Health Projects, PATH, et la FIGO, explore des stratégies pour aider les gouvernements et les partenaires améliorer la santé maternelle en élargissant laccès au misoprostol pour lhémorragie du post-partum (HPP), lune des principales causes de mortalité maternelle. Les principales stratégies pour introduire et élargir laccès au misoprostol pour le traitement et la prévention de lHPP comprennent : mettre en place une politique nationale favorable Inclure le misoprostol dans les budgets nationaux pour la santé ; préparer et diffuser des directives cliniques au niveau national Former les prestataires de santé ; assurer un approvisionnement et une distribution constants ; and sensibiliser les communautés et renforcer leur demand.. ...
Cette note dinformation stratégique, publié par la FCI en partenariat avec Gynuity Health Projects, PATH, et la FIGO, explore des stratégies pour aider les gouvernements et les partenaires améliorer la santé maternelle en élargissant laccès au misoprostol pour lhémorragie du post-partum (HPP), lune des principales causes de mortalité maternelle. Les principales stratégies pour introduire et élargir laccès au misoprostol pour le traitement et la prévention de lHPP comprennent : mettre en place une politique nationale favorable Inclure le misoprostol dans les budgets nationaux pour la santé ; préparer et diffuser des directives cliniques au niveau national Former les prestataires de santé ; assurer un approvisionnement et une distribution constants ; and sensibiliser les communautés et renforcer leur demand.. ...
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Misoprostol is an agonist for prostaglandin E receptor. Misoprostol is useful in treating patient with gastric ulcer due to NSAIDS.
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Misoprostol - Misoprostol is used for reducing the risk of stomach ulcers in patients who take nonsteroidal anti-inflammatory drugs (NSAIDs).
Cesarean scar pregnancy treated by curettage and aspiration guided by laparoscopy Shan-rong Shu, Xin Luo, Zhi-xin Wang, Yu-hong Yao Department of Obstetrics and Gynecology, The First Affiliated Hospital of JiNan University, HuangPu Road West, Guangzhou, Peoples Republic of China Abstract: Pregnancy in a cesarean scar is the rarest form of an ectopic pregnancy. The treatment for cesarean scar pregnancy mainly includes systemic methotrexate and uterine artery embolization. Here, we reported a case of cesarean scar pregnancy treated by curettage and aspiration guided by laparoscopy. The treatment plan included two phases. Three days after a combination of methotrexate and mifepristone was administered, the gestational sac was removed under laparoscopy, which enabled a successful treatment for the unruptured ectopic pregnancy in a previous cesarean scar and made it possible to preserve the reproductive capability of the patient. Keywords: cesarean scar pregnancy, laparoscopy, curettage and aspiration
Background & aim: Cervical ectopic pregnancy is a rare variant of ectopic pregnancy, and placenta percreta is a complex and dangerous condition; patients with these conditions are difficult to manage. In this study, we present a rare case of placenta percreta in cervical pregnancy. Case report: A 32 -year-old woman with 19 weeks of gestation and gross hematuria was admitted to Qaem Hospital in February 2014. Abdominal sonography and magnetic resonance findings indicated percreta. Cystoscopy was performed, which demonstrated invasion of placenta into bladder mucosa. Surgery was planned due to severe hematuria, where cervical ectopic pregnancy with placenta percreta was found. Hysterectomy and partial cystectomy were performed, and to date, the patient is alive and healthy. Conclusion:Placenta percreta with bladder invasion can cause hematuria during pregnancy and early diagnosis can help with successful treatment and management of bleeding.
TY - JOUR. T1 - Active management of term prelabour rupture of membranes with oral misoprostol. AU - Shetty, Ashalatha. AU - Stewart, K.. AU - Stewart, G.. AU - Rice, P.. AU - Danielian, P.. AU - Templeton, Alexander Allan. PY - 2002. Y1 - 2002. N2 - Objective To compare the active management of term prelabour rupture of membranes with oral misoprostol with conservative management for 24 hours followed by induction with oxytocin or prostaglandin E-2 (PGE(2)) gel.Design A non-blinded randomised controlled trial.Setting Induction and labour wards, Aberdeen Maternity Hospital.Population Sixty-one women with confirmed prelabour rupture of the membranes at , 36 weeks of gestation.Methods The women were randomised to 50 mug of oral misoprostol repeated every 4 hours, if required, to a maximum of five doses (active group), or to induction of labour with PGE2 gel or oxytocin only if not in spontaneous labour 24 hours after prelabour rupture of membranes (conservative group).Main outcome measures Number ...
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Ectopic pregnancy occurs at a rate of 19.7 cases per 1,000 pregnancies in North America and is a leading cause of maternal mortality in the first trimester. Greater awareness of risk factors and improved technology (biochemical markers and ultrasonography) allow ectopic pregnancy to be identified before the development of life-threatening events. The evaluation may include a combination of determination of urine and serum human chorionic gonadotropin (hCG) levels, serum progesterone levels, ultrasonography, culdocentesis and laparoscopy. Key to the diagnosis is determination of the presence or absence of an intrauterine gestational sac correlated with quantitative serum beta-subunit hCG (beta-hCG) levels. An ectopic pregnancy should be suspected if transvaginal ultrasonography shows no intrauterine gestational sac when the beta-hCG level is higher than 1,500 mlU per mL (1,500 IU per L). If the beta-hCG level plateaus or fails to double in 48 hours and the ultrasound examination fails to identify an
Group III: intracervical injection of hyaluronidase enzyme, referred hereafter as "Hyal.". Intervention. In Group I, PGE2 3 mg tablet was applied every 12 hours as a prostaglandin type to enhance cervical ripening and vaginal termination of pregnancy. If spontaneous contractions occurred every 2 minutes or if cervical score reached 9 or more, the next dose was not administered. If there were no effective uterine contractions after cervical score reaches 9, amniotomy with oxytocin IV infusion was commenced at a rate of 1 mU/min, and the infusion rate was doubled every 30 minutes until the uterine contractions become regular at 3-minute interval. If 48 hours passed without labor, it was considered method fail-ure, and in this situation, CS was offered for the patient.. In Group II, Foleys catheter no. 22 was inserted through the cervix under aseptic technique and pushed by uterine sound under ultrasound guide. The balloon was inflated by 30 mL normal saline, traction was applied to the catheter, ...
Some scientists say the vaginal insertion may introduce bacteria along with the drug. After examining many studies, the F.D.A. in 2000 approved a protocol that requires women to take misoprostol orally. But abortion providers have instead instructed women to insert misoprostol vaginally. The tablets are small, and women dont necessarily know where their vagina begins and ends, said Dr. Phillip G. Stubblefield, a professor of obstetrics and gynecology at Boston University. If women are not careful, Dr. Stubblefield said, they can easily drag the tablet across the perineum, between the rectum and vagina, and contaminate the vagina with the bacteria. Other experts dismissed the contamination idea. Im still using the vaginal route, said Dr. Mitchell Creinin, director of family planning at the University of Pittsburgh ...

Effects of Abatacept in Patients With Early Rheumatoid Arthritis - Full Text View - ClinicalTrials.govEffects of Abatacept in Patients With Early Rheumatoid Arthritis - Full Text View - ClinicalTrials.gov

Abortifacient Agents, Nonsteroidal. Abortifacient Agents. Reproductive Control Agents. Physiological Effects of Drugs. ... Antineoplastic Agents. Dermatologic Agents. Enzyme Inhibitors. Folic Acid Antagonists. Immunosuppressive Agents. Immunologic ...
more infohttps://clinicaltrials.gov/ct2/show/NCT02504268?term=Orencia&cond=%22Connective+Tissue+Disease%22&intr=%22Abatacept%22&rank=80

A Study of CNTO 136 (Sirukumab) Administered Subcutaneously in Japanese Patients With Active Rheumatoid Arthritis Unresponsive...A Study of CNTO 136 (Sirukumab) Administered Subcutaneously in Japanese Patients With Active Rheumatoid Arthritis Unresponsive...

Abortifacient Agents, Nonsteroidal. Abortifacient Agents. Reproductive Control Agents. Physiological Effects of Drugs. ... Antirheumatic Agents. Nucleic Acid Synthesis Inhibitors. Anti-Infective Agents. Anti-Inflammatory Agents, Non-Steroidal. ... Antineoplastic Agents. Dermatologic Agents. Enzyme Inhibitors. Folic Acid Antagonists. Immunosuppressive Agents. Immunologic ... If using nonsteroidal anti-inflammatory drugs (NSAIDs) or other analgesics (pain relievers) for RA, must be on a stable dose ...
more infohttps://clinicaltrials.gov/ct2/show/NCT01689532?recr=Open&cond=%22Arthritis%2C+Rheumatoid%22&rank=12

Methotrexate Treatment for Ectopic Pregnancy - Full Text View - ClinicalTrials.govMethotrexate Treatment for Ectopic Pregnancy - Full Text View - ClinicalTrials.gov

Abortifacient Agents, Nonsteroidal. Abortifacient Agents. Reproductive Control Agents. Physiological Effects of Drugs. ... Antineoplastic Agents. Dermatologic Agents. Enzyme Inhibitors. Folic Acid Antagonists. Immunosuppressive Agents. Immunologic ...
more infohttps://clinicaltrials.gov/ct2/show/NCT01855568?recr=Open&cond=%22Pregnancy%2C+Ectopic%22&rank=2

Treosulfan and Fludarabine Phosphate Before Donor Stem Cell Transplant in Treating Patients With Nonmalignant Inherited...Treosulfan and Fludarabine Phosphate Before Donor Stem Cell Transplant in Treating Patients With Nonmalignant Inherited...

Abortifacient Agents, Nonsteroidal. Abortifacient Agents. Reproductive Control Agents. Physiological Effects of Drugs. ... Antineoplastic Agents. Dermatologic Agents. Enzyme Inhibitors. Folic Acid Antagonists. Immunosuppressive Agents. Immunologic ...
more infohttps://www.clinicaltrials.gov/ct2/show/NCT00919503

A Study of Tocilizumab With or Without Methotrexate in Patients With Rheumatoid Arthritis. - Full Text View - ClinicalTrials.govA Study of Tocilizumab With or Without Methotrexate in Patients With Rheumatoid Arthritis. - Full Text View - ClinicalTrials.gov

Abortifacient Agents, Nonsteroidal. Abortifacient Agents. Reproductive Control Agents. Physiological Effects of Drugs. ... Antineoplastic Agents. Dermatologic Agents. Enzyme Inhibitors. Folic Acid Antagonists. Immunosuppressive Agents. Immunologic ...
more infohttps://www.clinicaltrials.gov/ct2/show/NCT01010503?cntry=SK&rank=41

Misoprostol administration in first-trimester pregnancies with embryonic demise reduces uterine arterial blood flow.Misoprostol administration in first-trimester pregnancies with embryonic demise reduces uterine arterial blood flow.

0/Abortifacient Agents, Nonsteroidal; 59122-46-2/Misoprostol From MEDLINE®/PubMed®, a database of the U.S. National Library of ... Abortifacient Agents, Nonsteroidal / administration & dosage*, adverse effects. Abortion, Induced. Abortion, Missed. ...
more infohttp://www.biomedsearch.com/nih/Misoprostol-administration-in-first-trimester/14738166.html

A Category Names List - Drug Information Portal - U.S. National Library of MedicineA Category Names List - Drug Information Portal - U.S. National Library of Medicine

Abortifacient Agents (16). Abortifacient Agents, Nonsteroidal (13) • Non-steroidal chemical compounds with abortifacient ... Non-Steroidal (0) see Anti-Inflammatory Agents, Non-Steroidal. Anti-Ulcer Agents (77) • Various agents with different action ... Anti-Inflammatory Agents, Non-Steroidal (251) • Anti-inflammatory agents that are non-steroidal in nature. In addition to anti- ... Anti-Mycobacterial Agents (0) see Anti-Bacterial Agents. Anti-Obesity Agents (24) • Agents that increase energy expenditure and ...
more infohttps://druginfo.nlm.nih.gov/drugportal/drug/categories

Medical versus surgical termination of pregnancy in primigravid women--is the next delivery differently at risk? A population...Medical versus surgical termination of pregnancy in primigravid women--is the next delivery differently at risk? A population...

Abortifacient Agents, Nonsteroidal / adverse effects. Abortifacient Agents, Steroidal / adverse effects. Abortion, Induced / ... 0/Abortifacient Agents, Nonsteroidal; 0/Abortifacient Agents, Steroidal; 0/Drug Combinations; 59122-46-2/Misoprostol; 84371-65- ...
more infohttp://www.biomedsearch.com/nih/Medical-versus-surgical-termination-pregnancy/23126244.html

A Category Names List - Drug Information Portal - U.S. National Library of MedicineA Category Names List - Drug Information Portal - U.S. National Library of Medicine

Abortifacient Agents (16). Abortifacient Agents, Nonsteroidal (13) • Non-steroidal chemical compounds with abortifacient ... Non-Steroidal (0) see Anti-Inflammatory Agents, Non-Steroidal. Anti-Ulcer Agents (78) • Various agents with different action ... Anti-Inflammatory Agents, Non-Steroidal (251) • Anti-inflammatory agents that are non-steroidal in nature. In addition to anti- ... Anti-Mycobacterial Agents (0) see Anti-Bacterial Agents. Anti-Obesity Agents (24) • Agents that increase energy expenditure and ...
more infohttps://druginfo.nlm.nih.gov/drugportal/jsp/drugportal/drugNamesAndCategories.jsp

RCSB PDB - MTX Ligand Summary PageRCSB PDB - MTX Ligand Summary Page

Abortifacient Agents. *Abortifacient Agents, Nonsteroidal. *Aminopterin. *Antimetabolites. *Antimetabolites, Antineoplastic. * ... Methotrexate is used alone or in combination with other anticancer agents in the treatment of breast cancer, epidermoid cancers ... Methotrexate is also used in combination with other chemotherapeutic agents in the treatment of advanced stage non-Hodgkins ... in the prophylaxis of meningeal leukemia and is used in maintenance therapy in combination with other chemotherapeutic agents. ...
more infohttps://www.rcsb.org/ligand/MTX

ChemIDplus - 59-05-2 - FBOZXECLQNJBKD-ZDUSSCGKSA-N - Methotrexate [USAN:USP:INN:BAN:JAN] - Similar structures search, synonyms,...ChemIDplus - 59-05-2 - FBOZXECLQNJBKD-ZDUSSCGKSA-N - Methotrexate [USAN:USP:INN:BAN:JAN] - Similar structures search, synonyms,...

Abortifacient Agents. *. Abortifacient Agents, Nonsteroidal. *. Agricultural Chemical. *. Antimetabolites. *. Antimetabolites, ...
more infohttps://chem.nlm.nih.gov/chemidplus/rn/59-05-2

Search Articles | University of Toronto LibrariesSearch Articles | University of Toronto Libraries

abortifacient agents, nonsteroidal - administration & dosage (93) 93 Filter by. Remove filter. drug therapy, combination (93) ... Anti-Bacterial Agents - therapeutic use , Early Termination of Clinical Trials , Glasgow Coma Scale , Adult , Female , Aged , ... Hypolipidemic Agents - adverse effects , Atorvastatin - adverse effects , Double-Blind Method , Nocebo Effect , Humans , Middle ... Antineoplastic Agents, Alkylating - therapeutic use , Glioblastoma - therapy , Canada , Disease-Free Survival , Electric ...
more infohttps://query.library.utoronto.ca/index.php/search/q?kw=SubjectTerms:Early%20Termination%20of%20Clinical%20Trials

Randomised trial of nitric oxide donor versus prostaglandin for cervical ripening before first-trimester termination of...Randomised trial of nitric oxide donor versus prostaglandin for cervical ripening before first-trimester termination of...

Abortifacient Agents, Nonsteroidal/adverse effects. *Abortifacient Agents, Nonsteroidal/therapeutic use*. *Abortion, Induced* ...
more infohttps://www.ncbi.nlm.nih.gov/pubmed/9798584

The Incidence of Menstrual Regulation Procedures and Abortion in Bangladesh, 2014.  - PubMed - NCBIThe Incidence of Menstrual Regulation Procedures and Abortion in Bangladesh, 2014. - PubMed - NCBI

Abortifacient Agents, Nonsteroidal/therapeutic use. *Abortion, Induced*/adverse effects. *Abortion, Induced*/methods ...
more infohttps://www.ncbi.nlm.nih.gov/pubmed/28930621?dopt=Abstract

Misoprostolum [Inn-Latin]
        -
        Oxytocics,  Anti-ulcer Agents,  Abortifacient Agents,  Prostaglandins,  ATC:A02BB01Misoprostolum [Inn-Latin] - Oxytocics, Anti-ulcer Agents, Abortifacient Agents, Prostaglandins, ATC:A02BB01

It is sometimes co-prescribed with non-steroidal anti-inflammatory drugs (NSAIDs) to prevent the occurrence of gastric ...
more infohttp://pharmacycode.com/Misoprostolum_%5BInn-Latin%5D.html

Search Articles | University of Toronto LibrariesSearch Articles | University of Toronto Libraries

Abortifacient Agents, Nonsteroidal , Placenta Accreta , Life Sciences , Santé publique et épidémiologie , Methotrexate ... Abortifacient Agents, Nonsteroidal - therapeutic use , Combined Modality Therapy , Hysterectomy , Methotrexate - therapeutic ...
more infohttps://query.library.utoronto.ca/index.php/search/q?kw=SubjectTerms:Placenta%20Accreta%20-%20therapy

Evidence Central | By Topic AEvidence Central | By Topic A

Abortifacient Agents. *Abortifacient Agents, Nonsteroidal. *Abortifacient Agents, Steroidal. *Abortion, Eugenic. *Abortion, ...
more infohttps://evidence.unboundmedicine.com/evidence/index/Cochrane/By_Topic/A

Liste alphabétique			- TermSciences
		Liste alphabétique - TermSciences

Abortifacient Agents. *Abortifacient Agents, Nonsteroidal. *Abortifacient Agents, Steroidal. *Air Abrasion, Dental. *Abreaction ...
more infohttp://inserm.termsciences.fr/-/Index/Explorer/Alphabet/

Adrenergic beta-AgonistsAdrenergic beta-Agonists

Abortifacient Agents. Abortifacient Agents, Nonsteroidal. Abortifacient Agents, Steroidal. ACE Inhibitors and Calcium Channel ...
more infohttp://www.genericdrugscan.com/drug-category/adrenergic-beta-agonists

Acetylcholine Release Inhibitors<span class=...Acetylcholine Release Inhibitors<span class=...

Abortifacient Agents. Abortifacient Agents, Nonsteroidal. Abortifacient Agents, Steroidal. ACE Inhibitors and Calcium Channel ...
more infohttp://www.genericdrugscan.com/drug-category/acetylcholine-release-inhibitors

conditions: Abconditions: Ab

Abortifacient Agents. *Abortifacient Agents, Non Steroidal. *Abortifacient Agents, Non-Steroidal. *Abortifacient Agents, ...
more infohttp://conditions.healthplace.com/sections/Ab

Antimicrobial drugs - definition of antimicrobial drugs by The Free DictionaryAntimicrobial drugs - definition of antimicrobial drugs by The Free Dictionary

aborticide, abortifacient, abortion-inducing drug - a drug (or other chemical agent) that causes abortion ... nonsteroidal antiinflammatory - (NSAID) antiinflamatorio no esteroideo (AINE); orphan - medicamento huérfano; prescription - ... Types of drug abirritant, abortifacient, ACE inhibitor, adjuvant, agrypnotic, alexipharmic, alkylating agent, alterative, ... anaesthetic, anaesthetic agent, anesthetic, anesthetic agent - a drug that causes temporary loss of bodily sensations ...
more infohttps://www.thefreedictionary.com/antimicrobial+drugs

List of MeSH codes (D16) - WikipediaList of MeSH codes (D16) - Wikipedia

... abortifacient agents MeSH D27.505.696.875.131.100 --- abortifacient agents, nonsteroidal MeSH D27.505.696.875.131.200 --- ... abortifacient agents MeSH D27.505.954.705.131.100 --- abortifacient agents, nonsteroidal MeSH D27.505.954.705.131.200 --- ... anti-inflammatory agents MeSH D27.505.954.158.030 --- anti-inflammatory agents, non-steroidal MeSH D27.505.954.158.030.500 --- ... antirheumatic agents MeSH D27.505.954.329.030 --- anti-inflammatory agents, non-steroidal MeSH D27.505.954.329.337 --- gout ...
more infohttps://en.wikipedia.org/wiki/List_of_MeSH_codes_(D16)

COX-2 inhibitors | definition of COX-2 inhibitors by Medical dictionaryCOX-2 inhibitors | definition of COX-2 inhibitors by Medical dictionary

Should not be used by patients who have shown allergic reactions to other non-steroidal anti-inflammatory agents such as ... However, misoprostol is an abortifacient and has been associated with birth defects. For this reason, it may be inappropriate ... Although the non-steroidal anti-inflammatory drugs are considered relatively safe, they are so widely used that their adverse ... a group of nonsteroidal antiinflammatory drugs (NSAIDs) that act by inhibiting cyclooxygenase-2 activity and have fewer GI side ...
more infohttp://medical-dictionary.thefreedictionary.com/COX-2+inhibitors

Global Library of Womens Medicine - Medical Termination of Early Pregnancy - DOI 10.3843/GLOWM.10443Global Library of Women's Medicine - Medical Termination of Early Pregnancy - DOI 10.3843/GLOWM.10443

Tang GW, Lau OWK, Yip P: Further acceptability evaluation of RU 486 and ONO 802 as abortifacient agents in a Chinese population ... Creinin MD, Shulman T: Effect of non-steroidal anti-inflammatory drugs on the action of misoprostol in a regimen for early ... The first evaluation of misoprostol alone as an abortifacient suggested that the agent, even when used vaginally, was ... Agents Used Currently for Medical Abortion. MIFEPRISTONE.. Background.. Progesterone is fundamentally important for sustaining ...
more infohttp://editorial.glowm.com/?p=glowm.cml/section_view&articleid=442
  • On September 30, 2004, the United States Food and Drug Administration announced that Merck and Company was withdrawing rofecoxib from the market, based on evidence from long-term studies showing that the drug had a higher risk of cardiovascular problems than comparable agents. (thefreedictionary.com)
  • Birth control pills (misoprostol)is usually given to patients of advanced age, as risk of ulcer development after use of nonsteroidal antiinflammatory drugs. (startstock.ru)
  • cytotec (misoprostol) is a drug that was originally developed as a medicinal product to protect the cavity of the stomach and d.Birth control pills (misoprostol)is usually given to patients of advanced age, as risk of ulcer development after use of nonsteroidal antiinflammatory drugs. (startstock.ru)
  • Moringa can raise the risk of bleeding when taken with drugs that increase the risk of bleeding like aspirin, anticoagulants (these are blood thinners), antiplatelet drugs like Plavix, naproxen (Aleve or Naprosyn) or nonsteroidal anti-inflammatory medicines like ibuprofen (Motrin or Advil). (voxnature.com)