Does PRAVASTATIN Cause Wrong technique in product usage process? 42 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Wrong technique in product usage process have been filed in association with PRAVASTATIN (Pravastatin Sodium). This represents 0.5% of all adverse event reports for PRAVASTATIN.
42
Reports of Wrong technique in product usage process with PRAVASTATIN
0.5%
of all PRAVASTATIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From PRAVASTATIN?
Of the 42 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAVASTATIN. However, 42 reports have been filed with the FAERS database.
What Other Side Effects Does PRAVASTATIN Cause?
Myalgia (1,290)
Arthralgia (570)
Dyspnoea (514)
Fatigue (500)
Drug hypersensitivity (493)
Diarrhoea (478)
Headache (448)
Pruritus (432)
Nausea (420)
Dizziness (413)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which PRAVASTATIN Alternatives Have Lower Wrong technique in product usage process Risk?
PRAVASTATIN vs PRAVASTATIN\PRAVASTATIN
PRAVASTATIN vs PRAZAXA
PRAVASTATIN vs PRAZEPAM
PRAVASTATIN vs PRAZIQUANTEL
PRAVASTATIN vs PRAZOSIN