Does RISEDRONATE Cause Product substitution issue? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Product substitution issue have been filed in association with RISEDRONATE (Risedronate Sodium). This represents 0.7% of all adverse event reports for RISEDRONATE.
45
Reports of Product substitution issue with RISEDRONATE
0.7%
of all RISEDRONATE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product substitution issue From RISEDRONATE?
Of the 45 reports, 2 (4.4%) required hospitalization.
Is Product substitution issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISEDRONATE. However, 45 reports have been filed with the FAERS database.
What Other Side Effects Does RISEDRONATE Cause?
Drug hypersensitivity (1,124)
Asthma (1,087)
Pain (973)
Vomiting (971)
Drug ineffective (919)
Dyspnoea (898)
Pneumonia (807)
Wheezing (772)
Oedema (708)
Malaise (668)
What Other Drugs Cause Product substitution issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832)
BUPROPION (1,578)
METHYLPHENIDATE (1,408)
CLONAZEPAM (1,288)
LAMOTRIGINE (979)
ALBUTEROL (864)
LEVOTHYROXINE (803)
DULOXETINE (766)
ESTRADIOL (692)
SERTRALINE (636)
Which RISEDRONATE Alternatives Have Lower Product substitution issue Risk?
RISEDRONATE vs RISEDRONIC ACID
RISEDRONATE vs RISPERDAL
RISEDRONATE vs RISPERDAL CONSTA
RISEDRONATE vs RISPERIDONE
RISEDRONATE vs RITALIN