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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PAROXETINE Cause Psychomotor hyperactivity? 84 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Psychomotor hyperactivity have been filed in association with PAROXETINE (Paroxetine). This represents 0.4% of all adverse event reports for PAROXETINE.

84
Reports of Psychomotor hyperactivity with PAROXETINE
0.4%
of all PAROXETINE reports
9
Deaths
55
Hospitalizations

How Dangerous Is Psychomotor hyperactivity From PAROXETINE?

Of the 84 reports, 9 (10.7%) resulted in death, 55 (65.5%) required hospitalization, and 5 (6.0%) were considered life-threatening.

Is Psychomotor hyperactivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 84 reports have been filed with the FAERS database.

What Other Side Effects Does PAROXETINE Cause?

Foetal exposure during pregnancy (1,894) Drug ineffective (1,457) Toxicity to various agents (1,407) Drug abuse (1,214) Anxiety (1,201) Nausea (1,063) Suicidal ideation (999) Drug interaction (991) Confusional state (975) Dizziness (937)

What Other Drugs Cause Psychomotor hyperactivity?

METHYLPHENIDATE (617) QUETIAPINE (412) ARIPIPRAZOLE (389) OLANZAPINE (366) SERTRALINE (288) MONTELUKAST (282) RISPERIDONE (277) LEVETIRACETAM (247) VENLAFAXINE (214) LEVOTHYROXINE (211)

Which PAROXETINE Alternatives Have Lower Psychomotor hyperactivity Risk?

PAROXETINE vs PAROXETINE\PAROXETINE PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS PAROXETINE vs PASIREOTIDE PAROXETINE vs PASIREOTIDE DIASPARTATE PAROXETINE vs PATIROMER

Related Pages

PAROXETINE Full Profile All Psychomotor hyperactivity Reports All Drugs Causing Psychomotor hyperactivity PAROXETINE Demographics