221. Metabolic effects of a long acting injectable steroid contraceptive

1978 ◽  
Vol 9 (9) ◽  
pp. 859
Author(s):  
M Tankeyoon ◽  
N. Dusitsin ◽  
V. Poshyachinda ◽  
S. Chompootaweep
2019 ◽  
Vol 25 (1) ◽  
Author(s):  
ASHOK KUMAR ◽  
ALPANA PARMAR ◽  
ANAND KUMAR BAJPEYEE

Young female Black rat (Rattus rattus), were administered monthly long acting steroid contraceptive to induce hypertriglyceridemia. It was observed that by 3 weeks of the second injection of estrogen containing mixed type of contraceptive, female rats developed consistent and frank hyperglyceridemia . TG in the treated rats was 195.8 ± 7.44 mg /100 ml as compared to 91.5 ± 6.27 mg/100ml in plasma of the control group.


Diabetes ◽  
1989 ◽  
Vol 38 (6) ◽  
pp. 704-709 ◽  
Author(s):  
K. Osei ◽  
T. M. O'Dorisio ◽  
W. B. Malarkey ◽  
E. L. Craig ◽  
S. Cataland

2009 ◽  
Vol 195 (S52) ◽  
pp. s13-s19 ◽  
Author(s):  
David Taylor

BackgroundDepot antipsychotics are widely used in clinical practice. Long-acting formulations of second-generation antipsychotics are now being developed and introduced.AimsTo review the pharmacology, pharmacokinetics and adverse effect profiles of currently available antipsychotic long-acting injections (LAIs).MethodThe psychopharmacological properties of first- and second-generation antipsychotic LAIs are reviewed using data available up to October 2008.ResultsFirst-generation antipsychotic (FGA) LAIs are associated with a high rate of acute and chronic movement disorders. Risperidone LAI is better tolerated in this respect, but is associated with hyperprolactinaemia and weight gain. Olanzapine LAI causes weight gain and other metabolic effects but appears not to be associated with an important incidence of movement disorders.ConclusionsDosing of LAIs is complicated by delayed release of drug, changes in plasma levels without change in dose, and by the lack of data establishing clear dose requirements. All LAIs offer the prospect of assured adherence (although patients may still default on treatment) but their use is complicated by adverse effects, complex pharmacokinetics and confusion over dose–response relationships.


Diabetes ◽  
1989 ◽  
Vol 38 (6) ◽  
pp. 704-709 ◽  
Author(s):  
K. Osei ◽  
T. M. O'Dorisio ◽  
W. B. Malarkey ◽  
E. L. Craig ◽  
S. Cataland

2015 ◽  
Vol 29 (12) ◽  
pp. 1280-1289 ◽  
Author(s):  
Kari M Ersland ◽  
Silje Skrede ◽  
Therese H Røst ◽  
Rolf K Berge ◽  
Vidar M Steen

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