Verapamil hydrochloride 120 mg tablets for 3 weeks; months after termination therapy, patient has no further relapse.
Patients:
Clinical Features: (1) Pain: (2) Pain was moderate to severe; it occurred mainly at night. (3) Dyspnea: (4) Dyspnea developed during the morning, with symptoms in morning lasting for 3 to 4 hours. (5) Respiratory: (6) dyspnea persisted to 3 months of maintenance therapy. (7) Diarrhea: (8) Abdominal pain.
Dosage:
A total amount not to exceed 100 mg daily.
CONTRAINDICATIONS
Contraindications: The use of cyclosporine has been associated with hepatotoxicity. These adverse effects may be aggravated by concomitant use of other drugs that cause a decrease in platelet aggregation such as raloxifene, ritonavir, and rifampin; concomitant use of cyclosporine with other agents that also decrease platelet aggregation including rifampin, amiodarone, fluconazole, terfenadine, and warfarin.
Warnings or Precautions:
Pseudoephedrine or arylcyclosporine may increase the incidence of hypersensitivity reactions. use an antipsychotic medication, other than clozapine, for more 6 months during antipsychotic therapy should be avoided; this will reduce the risk of psychotic reactions that are associated with antipsychotic exposure.
Risk of CNS Depression
The risk of developing a major depressive episode after discontinuation has not been systematically evaluated in clinical trials. If a major depressive episode has occurred during treatment with a psychiatric drug, discontinuance should be considered within 1 week.
Concomitant use of an MAOI with drugs that are CNS depressants or have a mechanism of action that is also a CNS depressant may result in serotonin syndrome. Caution is advised when coingestion of an MAOI and benzodiazepines, ethanol, opioids, barbiturates, clonazepam, and tricyclic antidepressants.
Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
Listed below are adverse reaction rates observed during treatment using sertraline (Zoloft, Sertraline).
Percent of population with a single adverse reaction (n = 3):
Adverse Reaction Percent of Population Rate Adverse Reaction sertraline 0.10 5.5
The adverse reaction rates presented above are those estimated to have occurred in at least 1 patient a given trial; they are not specific, and adverse reaction rates in patients assigned to receive the drug allure magazine best drugstore eye cream for an extended periods may be substantially higher.
Information supplied with or obtained from this Patient Information leaflet is believed to be accurate, but is not guaranteed. The FDA cautions patients that use of any drug requires that they know their specific medical conditions, that they periodically examine their medical condition, and that they should read the FDA-approved patient labeling with any drug they use.
The patient information leaflet is a publication of AmerisourceBergen Corporation.
This leaflet is available in the following languages:
AmerisourceBergen
AmerisourceBergen:
English: 877-929-0228
Franﾃｧais: 877-929-0229
Italiano: 877-929-0090
Espaﾃｱol: 877窶�929-0090
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