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1.
Article in French | MEDLINE | ID: mdl-6520357

ABSTRACT

TwO cases of megaloblastic anaemia, of which one was very severe, occurring in women who had been taking oestrogen-progestogen oral contraception over a long period of time, are reported. The authors take the opportunity, after having reviewed the literature, of pointing out the role of oestro-progestogen products in bringing about vitamin deficiencies. They discuss how and where oestrogen-progestogen products work on folic metabolism and emphasize that there is an associated factor which starts off the deficiencies.


Subject(s)
Anemia, Macrocytic/chemically induced , Anemia, Megaloblastic/chemically induced , Contraceptives, Oral, Combined/adverse effects , Contraceptives, Oral/adverse effects , Adult , Ethinyl Estradiol/adverse effects , Female , Humans , Norgestrel/adverse effects , Norgestrienone/adverse effects
4.
Contraception ; 18(4): 429-40, 1978 Oct.
Article in English | MEDLINE | ID: mdl-720075

ABSTRACT

Norgestrienone implants delivering approximately 225 microgram/ day were tested clinically for contraceptive effectiveness and acceptability in 145 women. Five pregnancies occurred in 2259 woman-months of use, one in the 11th month, one in the 15th and three in the 16th month of use. Continuation rate at 12 months was 86.7. The number of bleeding runs and bleeding days was increased in approximately 12% of the subjects. Ten percent of the patients had no bleeding in the first 90 days of treatment. Changes in bleeding pattern led to closures in four cases. Headache and signs of mild androgenicity were among the leading side effects. Blood and urine analysis throughout the study showed normal values of 17 different parameters, but a tendency to lower cholesterolemia not associated with changes in thyroid hormone levels, was observed in several patients. Cortisol was found slightly under the lower normal range in one subject without clinical manifestations of hypoadrenalism. It is concluded that norgestrienone implants should be replaced every twelve months for maximal contraceptive effect and because of their efficacy and good acceptability, evaluation of their long term use is warranted.


Subject(s)
Contraceptive Agents, Female/pharmacology , Norgestrienone/administration & dosage , Norpregnatrienes/administration & dosage , Adolescent , Adult , Cholesterol/blood , Drug Implants , Female , Humans , Hydrocortisone/blood , Menstruation/drug effects , Norgestrienone/adverse effects , Pregnancy , Silicone Elastomers , Time Factors
5.
Contraception ; 18(4): 315-33, 1978 Oct.
Article in English | MEDLINE | ID: mdl-363345

ABSTRACT

This paper presents results of a double blind, multi-centered and multi-national study of two progestin only subdermal implants used for contraception. A regimen of six capsules of levonorgestrel (Ng) used by 492 women had a net cumulative 12-month pregnancy rate of 0.6 percent and a continuation rate of 74.6 percent. 498 women used six capsules of norgestrienone (R2010) and experienced a net cumulative 12-month pregnancy rate of 3.5 percent and a continuation rate of 79.4 percent. The difference in the pregnancy rate was significant at P less than 0.01, while there was no significant difference in the continuation rates. Menstrual problems were the principal reason for termination of the levonorgestrel regimen, accounting for approximately half of all terminations. There were significantly fewer menstrual problems among users of the norgestrienone (R2010) capsules; the net cumulative 12-month termination rate for this reason was 4.3 percent. Results are compared with continuation and termination rates for acceptors of the Copper T 200 at the same clinics. The low pregnancy rate and reasonably high continuation rate of the norgestrel implants coupled with the fact that the expected effective lifetime of a set of capsules is of the order of 3-5 years appears to warrant further development of this contraceptive regimen.


Subject(s)
Megestrol/pharmacology , Norgestrel/pharmacology , Norgestrienone/pharmacology , Norpregnatrienes/pharmacology , Adolescent , Adult , Body Weight , Clinical Trials as Topic , Double-Blind Method , Drug Implants , Female , Humans , International Cooperation , Intrauterine Devices, Copper , Norgestrel/adverse effects , Norgestrienone/adverse effects , Pregnancy , Time Factors
7.
Ann Endocrinol (Paris) ; 38(6): 361-2, 1977.
Article in French | MEDLINE | ID: mdl-206178

ABSTRACT

A new case report of primary malignant hepatic tumor during a long term oral contraception is presented. A direct role of contraceptives drugs cannot be claimed because of little cases reported. Nevertheless, appearance of carcinogenic compounds in predisposed women may be evoked.


PIP: The article describes the case of a 42 year old woman who died of liver cell carcinoma; the woman had been on oral contraceptives (OCs) for 10 years. The association between OCs and liver cancer is being reported more and more frequently. Still, it is not clear exactly which is the mechanism that causes the malignant tumor. If coincidence and preexisting tumor are ruled out, it is possible that OCs, diminishing biliar excretion, help the accumulation of carcinogenetic substances.


Subject(s)
Carcinoma, Hepatocellular/chemically induced , Contraceptives, Oral, Hormonal/adverse effects , Contraceptives, Oral/adverse effects , Liver Neoplasms/chemically induced , Adult , Estradiol/adverse effects , Female , Humans , Mestranol/adverse effects , Norgestrel/adverse effects , Norgestrienone/adverse effects
9.
Contraception ; 12(3): 299-307, 1975 Sep.
Article in English | MEDLINE | ID: mdl-1164848

ABSTRACT

PIP: The effect of progestin R 2323 released from intravaginal rings (IVR) on ovarian function was studied in 20 young healthy volunteers. The silastic IVRs containing 10, 20, 50, or 200 mg of progestin R 2323 were inserted on the 1st day after menstrual bleeding and removed 21 days after insertion. The IVRs were tolerated well without irritation or alteration of the vaginal mucosa. Control plasma estradiol and progesterone levels revealed 18 of 20 cycles were ovulatory. No ovulation was observed during treatment, as revealed by consistently suppressed progesterone levels. Normal ovulation resumed after removal of the rings. 3 women experienced withdrawal bleeding; 9 had breakthrough bleeding and 13 had a normal postovulatory bleeding 15-33 days after ring removal. It was concluded that the bleeding control was unsatisfactory with every dosage of R 2323 used in this study.^ieng


Subject(s)
Norgestrienone/pharmacology , Norpregnatrienes/pharmacology , Ovary/drug effects , Adult , Contraceptive Devices, Female , Delayed-Action Preparations , Estradiol/blood , Female , Humans , Menstruation Disturbances/chemically induced , Norgestrienone/adverse effects , Norgestrienone/analogs & derivatives , Ovary/physiology , Progesterone/blood , Vagina/drug effects
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