TABLE 6.
Summary of nonconvergent data
| Preclinical | Clinical | Comments | |
|---|---|---|---|
| Birth defects | No substantial evidence | Sporadic case reports and statistical evidence of increased risk in some large scale studies. | Numerous potential confounds in clinical literature preclude conclusions in the presence of prolonged record of antidepressant use during pregnancy (>40 years). | 
| Long-term outcome | No persistent adverse effects | Limited studies from neonatal to early childhood do not demonstrate significant risk. No studies of long-term outcomes in offspring into adolescence or adulthood. | Preclinical studies of postnatal exposure reveal long term behavioral alterations, however many findings are not replicable. Clinical relevancy of dosing regimens must be taken into account. | 
| Monoamine/neuroendocrine | Altered monoamine | Altered salivary cortisol in children | Preclinical studies may have questionable dosing relevancy | 
| Altered cortisol and insulin | |||
| Behavioral outcome | Some evidence for behavioral outcome | Some studies show behavioral differences in children | Preclinical studies of postnatal exposure reveal long term behavioral alterations | 
| Studies often conflicting or not replicated |