

Special Alerts:
[Posted 02/22/2011] ISSUE: FDA notified healthcare professionals that the Pregnancy section of drug labels for the entire class of antipsychotic drugs has been updated. The new drug labels now contain more and consistent information about the potential risk for abnormal muscle movements (extrapyramidal signs or EPS) and withdrawal symptoms in newborns whose mothers were treated with these drugs during the third trimester of pregnancy.
The symptoms of EPS and withdrawal in newborns may include agitation, abnormally increased or decreased muscle tone, tremor, sleepiness, severe difficulty breathing, and difficulty in feeding. In some newborns, the symptoms subside within hours or days and do not require specific treatment; other newborns may require longer hospital stays.
BACKGROUND: Antipsychotic drugs are used to treat symptoms of psychiatric disorders such as schizophrenia and bipolar disorder.
RECOMMENDATION: Healthcare professionals should be aware of the effects of antipsychotic medications on newborns when the medications are used during pregnancy. Patients should not stop taking these medications if they become pregnant without talking to their healthcare professional, as abruptly stopping antipsychotic medications can cause significant complications for treatment. For more information visit the FDA website at: [Web] and [Web].
[Posted 06/16/2008] FDA notified healthcare professionals that both conventional and atypical antipsychotics are associated with an increased risk of mortality in elderly patients treated for dementia-related psychosis. In April 2005, FDA notified healthcare professionals that patients with dementia-related psychosis treated with atypical antipsychotic drugs are at an increased risk of death. Since issuing that notification, FDA has reviewed additional information that indicates the risk is also associated with conventional antipsychotics. Antipsychotics are not indicated for the treatment of dementia-related psychosis. The prescribing information for all antipsychotic drugs will now include the same information about this risk in a BOXED WARNING and the WARNINGS section. For more information visit the FDA website at: [Web], [Web] and [Web].
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![]() | 832 50 50 mg bottle, 100 each Chlorpromazine HCl 50mg, Oral tablet, brown, biconvex, round-shaped, side 1:832 50 |
![]() | GG 476 | 25 25 mg bottle, 100 each Chlorpromazine HCl 25mg, Oral tablet, orange, round-shaped, side 1:GG 476, side 2:25 |
![]() | 10 | GG 455 10 mg bottle, 100 each Chlorpromazine HCl 10mg, Oral tablet, orange, round-shaped, side 1:10, side 2:GG 455 |
![]() | 832 10 10 mg bottle, 100 each Chlorpromazine HCl 10mg, Oral tablet, brown, biconvex, round-shaped, side 1:832 10 |
![]() | GG 407 | 50 50 mg bottle, 100 each Chlorpromazine HCl 50mg, Oral tablet, orange, round-shaped, side 1:GG 407, side 2:50 |
![]() | GG 437 | 100 100 mg bottle, 100 each Chlorpromazine HCl 100mg, Oral tablet, orange, round-shaped, side 1:GG 437, side 2:100 |
![]() | 832 100 100 mg bottle, 100 each Chlorpromazine HCl 100mg, Oral tablet, brown, biconvex, round-shaped, side 1:832 100 |
![]() | GG 457 | 200 200 mg bottle, 100 each Chlorpromazine HCl 200mg, Oral tablet, orange, round-shaped, side 1:GG 457, side 2:200 |



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