| Risperdal Dosages & Strengths | ||||
|---|---|---|---|---|
| Strength | Format | Route | Strength | Class |
| Risperdal 0.5 mg | tablet | oral | 1.0 each | OTC |
| Risperdal 3 mg | tablet | oral | 1.0 each | OTC |
| Risperdal 0.25 mg | tablet | oral | 1.0 each | OTC |
| Risperdal 1 mg | tablet | oral | 1.0 each | OTC |
| Risperdal 2 mg | tablet | oral | 1.0 each | OTC |
| Risperdal 4 mg | tablet | oral | 1.0 each | OTC |
| Risperdal 1 mg/mL | solution | oral | 1.0 milliliter(s) | OTC |
Posted by nomoremeds about 1 month ago
Risperdal increases production of prolactin. That would explain lactation and reduced sex drive. So if you read that it doe...
Posted by nomoremeds about 1 month ago
It was like having the munchies when you smoke weed.
Posted by nomoremeds about 1 month ago
I tried SO HARD not to overeat, but I was SO HUNGRY.
Teva Wants the FDA to Do What? - Motley Fool
In 2001 Teva filed a marketing application for its generic version of Risperdal claiming that J&J's patent was invalid. Later that year, the FDA removed the ...
Wed Mar 05 15:17:40 -0500 2008
Teva files suit against FDA to relist generic risperdal - CNNMoney.com
Risperdal is an antipsychotic medication used to treat schizophrenia and manic states associated with bipolar disorder. The copying, republication or ...
Wed Mar 05 02:38:33 -0500 2008
Teva files suit against FDA to relist generic risperdal - Interactive Investor
Risperdal is an antipsychotic medication used to treat schizophrenia and manic states associated with bipolar disorder. tf.TFN-Europe_newsdesk@thomson.com ...
Wed Mar 05 02:53:18 -0500 2008
risperidone - A benzisoxazole derivative with antipsychotic property. Risperidone selectively antagonizes serotonin (5-HT) effects via cortical 5-HT2 receptor, and, to a lesser extent, competes with dopamine at the limbic dopamine D2 receptor. The antagonism leads to decreased psychotic effects, such as hallucinations and delusions. In addition, risperidone has low to moderate affinity for histamine H1, 5-HT1A, 5-HT1C, and 5-HT1D receptors, while it has weak affinity for dopamine D1 and haloperidol-sensitive sigma site receptors.