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Department of Reproductive Health and Research (RHR), World Health Organization
A guide to essential practice
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Annexes Medications in pregnancy During pregnancy, the mother and the fetus form one biological unit,
and the health of the fetus depends on the health of the mother. It is
important to treat the mother whenever needed, while protecting the
unborn baby to the greatest possible extent. Drugs can have harmful effects on the fetus at any time during
pregnancy. During the first trimester, drugs may produce congenital
malformations (teratogenesis); the greatest risk is between the third
and the eleventh week of pregnancy. Few drugs have been shown
conclusively to be teratogenic in humans but no drug is safe beyond all
doubt in early pregnancy. Drugs should be prescribed for a pregnant woman only if the expected
benefits to her are thought to be greater than the risk to the fetus.
All drugs should be avoided, if possible, during the first trimester.
Drugs that have been used extensively in pregnancy and appear to be
usually safe should be prescribed in preference to new or untried drugs
and the smallest effective dose should be used. The following list
includes information about use of some common drugs in pregnancy.
Absence of a drug from the list does not imply that it is safe. acyclovir Not known to be harmful; limited absorption from
topical preparations amoxicillin No evidence of teratogenicity ampicillin Not known to be harmful azithromycin Limited data in pregnancy; use only if potential
benefit outweighs risk. benzathine benzylpenicillin Not known to be harmful benzylpenicillin Not known to be harmful cefixime Single dose of cefixime is considered safe in
pregnancy ceftazidime Not known to be harmful ceftriaxone Not known to be harmful chloramphenicol Third trimester: neonatal "grey baby" syndrome ciprofloxacin Avoid�arthropathy in animal studies; safer
alternatives available clindamycin Not known to be harmful clotrimazole Not studied in first trimester. Used vaginally
during second and third trimester not shown to cause birth defects. cloxacillin Not known to be harmful doxycycline Contraindicated in pregnancy and breastfeeding: First trimester: effects on skeletal development in
animal studies Second and third trimesters: dental discoloration in
children; maternal hepatotoxicity with large parenteral doses erythromycin Not known to be harmful famciclovir Animal studies did not show any risk for fetus�use
only when potential benefit outweighs risk fluconazole Avoid in first trimester�multiple congenital
abnormalities reported with long-term high doses gentamicin Second and third trimesters: auditory or vestibular
nerve damage; risk probably very small, but use only if potential
benefit outweighs risk (if given, monitoring of serum gentamicin
concentration essential) metronidazole First trimester: avoid Second and third trimesters: avoid high-dose
regimens (>1g) nystatin No information available, but absorption from
gastrointestinal tract negligible ofloxacin Avoid�arthropathy in animal studies; safer
alternatives available podophyllum resin Avoid�neonatal death and teratogenesis have been
reported streptomycin Second and third trimesters: auditory or vestibular
nerve damage; avoid unless essential (if given, monitoring of serum
streptomycin concentration essential) sulfamethoxazole + trimethoprim First trimester: theoretical teratogenic risk (trimethoprim
is a folate antagonist) Third trimester: neonatal haemolysis and
methaemoglobinaemia; suggestion of increased risk of kernicterus in
neonates appears to be unfounded tinidazole Manufacturer advises to avoid in first trimester Second and third trimesters: avoid high-dose
regimens (>1g) tetracycline Contraindicated in pregnancy and breastfeeding: First trimester: effects on skeletal development in
animal studies Second and third trimesters: dental discoloration in
children; maternal hepatotoxicity with large parenteral doses trimethoprim First trimester: theoretical teratogenic risk (folate
antagonist) valaciclovir Animal studies did not show any risk for fetus�use
only when potential benefit outweighs risk; vancomycin Use only if potential benefit outweighs
risk�monitoring of plasma vancomycin concentration essential to
reduce risk of fetal toxicity zidovudine and other antiretrovirals Avoid if possible in first trimester; benefit of
treatment considered to outweigh risk in second and third trimesters Antibiotic
treatments for gonorrhoea
WHO recommended treatments for urogenital and rectal
gonorrhoea Dosage Safe in pregnancy? Resistance cefixime 400 mg orally as a single dose Yes No ceftriaxone 125 mg by intramuscular injection Yes No ciprofloxacina 500 mg orally as a single dose No Extensive quinolone resistance in parts of the WHO
South-East Asia and Western Pacific Regions spectinomycin 2 g by intramuscular injection Yes No Other effective treatments for urogenital and rectal
gonorrhoea cefotaxime 1 g by intramuscular injection Yes No ceftizoxime 1 g by intramuscular injection Yes No cefuroxime 1.5 g by intramuscular injection Yes No levofloxacina 250 mg orally as a single dose No Extensive quinolone resistance in parts of the WHO
South-East Asia and Western Pacific Regions norfloxacina 400 mg orally as a single dose No ofloxacina 400 mg orally as a single dose No trimethoprim/ sulfamethoxazole 80/400 mg orally, 10 tablets as a single dose each
day for 3 days No Resistance in many regions a. The use of quinolones should take into consideration
the patterns of Neisseria gonorrhoeae resistance, such as in the WHO
South-East Asia and Western Pacific Regions. Treatment of gonorrhoea: 30 regimens, involving 21 antimicrobial
drugs have been shown to be effective for rectal and urogenital
infections. Few regimens have been shown to be highly effective against
pharyngeal infections. Among those antimicrobial agents available for
the treatment of uncomplicated gonococcal infections, ceftriaxone (125
mg), cefixime (400 mg), ciprofloxacin (500 mg), and ofloxacin (400 mg)
appear to offer the best balance of proven efficacy and safety. ____________________________ 1 Thirteenth WHO model list of essential drugs. Geneva,
World Health Organization, 2003. |
Contents
Infections of the male and female reproductive tract and their consequences: The role of clinical services in reducing the burden of STI/RTI Preventing STIs/RTIs and their complications How to prevent iatrogenic infections How to prevent endogenous infections Detecting STI/RTI STI/RTI education and counselling General skills for STI/RTI education and counselling Promoting prevention of STI/RTI and use of services Reducing barriers to use of services Raising awareness and promoting services Reaching groups that do not typically use reproductive health services STI/RTI Assessment during Routine Family Planning Visits Integrating STI/RTI assessment into routine FP services Family planning methods and STIs/RTIs STI/RTI Assessment in pregnancy, childbirth and the postpartum period Management of symptomatic STIs/RTIs Syndromic management of STI/RTI Management of common syndromes STI case management and prevention of new infections STI/RTI complications related to pregnancy, miscarriage, induced abortion, and the postpartum period Infection following childbirth Vaginal discharge in pregnancy and the postpartum period Sexual violence Medical and other care for survivors of sexual assault Annex 1. Clinical skills needed for STI/RTI Annex 2. Disinfection and universal precautions Preventing infection in clinical settings High-level disinfection: three steps Annex 3. Laboratory tests for RTI Interpreting syphilis test results Clinical criteria for bacterial vaginosis (BV) Gram stain microscopy of vaginal smears Use of Gram stain for diagnosis of cervical infection Annex 4. Medications Antibiotic treatments for gonorrhoa Annex 5. --------
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