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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 LAROTRECTINIB Cause Withdrawal syndrome? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Withdrawal syndrome have been filed in association with LAROTRECTINIB (VITRAKVI). This represents 0.9% of all adverse event reports for LAROTRECTINIB.

7
Reports of Withdrawal syndrome with LAROTRECTINIB
0.9%
of all LAROTRECTINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Withdrawal syndrome From LAROTRECTINIB?

Of the 7 reports, 1 (14.3%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Withdrawal syndrome Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LAROTRECTINIB. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does LAROTRECTINIB Cause?

Fatigue (56) Drug ineffective (52) Dizziness (50) Death (48) Pain (42) Neuropathy peripheral (39) Nausea (32) Off label use (31) Disease progression (27) Malignant neoplasm progression (23)

What Other Drugs Cause Withdrawal syndrome?

ACETAMINOPHEN\OXYCODONE (4,046) PREGABALIN (3,329) OXYCODONE (2,798) ACETAMINOPHEN\HYDROCODONE (2,636) FENTANYL (1,948) MORPHINE (1,674) TRAMADOL (1,582) VENLAFAXINE (1,516) DULOXETINE (1,328) BUPRENORPHINE (1,266)

Which LAROTRECTINIB Alternatives Have Lower Withdrawal syndrome Risk?

LAROTRECTINIB vs LASILIX LAROTRECTINIB vs LASIX LAROTRECTINIB vs LASMIDITAN LAROTRECTINIB vs LATANOPROST LAROTRECTINIB vs LATANOPROSTENE BUNOD

Related Pages

LAROTRECTINIB Full Profile All Withdrawal syndrome Reports All Drugs Causing Withdrawal syndrome LAROTRECTINIB Demographics