PELARGONIUM SIDOIDES

N/A

Manufactured by Schwabe North America

71 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PELARGONIUM SIDOIDES

PELARGONIUM SIDOIDES is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Schwabe North America. The most commonly reported adverse reactions for PELARGONIUM SIDOIDES include ASTHENIA, BLOOD PRESSURE INCREASED, DIZZINESS, DRUG DEPENDENCE, DRUG-INDUCED LIVER INJURY. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PELARGONIUM SIDOIDES.

Top Adverse Reactions

ASTHENIA2 reports
BLOOD PRESSURE INCREASED2 reports
DIZZINESS2 reports
DRUG DEPENDENCE2 reports
DRUG INDUCED LIVER INJURY2 reports
HEPATOTOXICITY2 reports
LIVER DISORDER2 reports
PNEUMONIA2 reports
ABDOMINAL DISCOMFORT1 reports
ACUTE HEPATIC FAILURE1 reports
ALCOHOLIC LIVER DISEASE1 reports
ALLERGIC GRANULOMATOUS ANGIITIS1 reports
ANAEMIA1 reports
ANXIETY1 reports
BACK PAIN1 reports
BASILAR ARTERY OCCLUSION1 reports
BRAIN STEM INFARCTION1 reports
CEREBRAL ARTERY EMBOLISM1 reports
CERVICAL SPINAL STENOSIS1 reports
CHEST DISCOMFORT1 reports
CHOLANGITIS1 reports
COMA1 reports
CONDITION AGGRAVATED1 reports
CORONARY ARTERY OCCLUSION1 reports
COUGH1 reports
DEATH1 reports
DEPRESSED LEVEL OF CONSCIOUSNESS1 reports
DRUG HYPERSENSITIVITY1 reports
DRUG INEFFECTIVE1 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION1 reports
DRUG INTERACTION1 reports
DYSPEPSIA1 reports
ELECTROCARDIOGRAM T WAVE INVERSION1 reports
FALL1 reports
FATIGUE1 reports
FEELING ABNORMAL1 reports
GASTROINTESTINAL INFECTION1 reports
GASTROOESOPHAGEAL REFLUX DISEASE1 reports
ILLNESS1 reports
INFLUENZA1 reports
INITIAL INSOMNIA1 reports
INSOMNIA1 reports
INTERSTITIAL LUNG DISEASE1 reports
LIVER INJURY1 reports
LOCKED IN SYNDROME1 reports
MUSCULOSKELETAL PAIN1 reports
MYDRIASIS1 reports
PANCREATITIS ACUTE1 reports
PERICARDIAL EFFUSION1 reports
PERIPHERAL EMBOLISM1 reports
PNEUMOTHORAX1 reports
PRODUCT DOSE OMISSION ISSUE1 reports
PUPILLARY REFLEX IMPAIRED1 reports
RESPIRATORY DISORDER1 reports
RESPIRATORY DISTRESS1 reports
RESPIRATORY FAILURE1 reports
SYNCOPE1 reports
TACHYCARDIA1 reports
TINNITUS1 reports
TYPE 2 DIABETES MELLITUS1 reports
UPPER LIMB FRACTURE1 reports
URINARY RETENTION1 reports
VIRAL INFECTION1 reports

Report Outcomes

Out of 22 classified reports for PELARGONIUM SIDOIDES:

Serious 81.8%Non-Serious 18.2%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female12 (54.5%)
Male10 (45.5%)

Reports by Age

Age 463 reports
Age 361 reports
Age 391 reports
Age 441 reports
Age 521 reports
Age 541 reports
Age 561 reports
Age 571 reports
Age 591 reports
Age 621 reports
Age 631 reports
Age 671 reports
Age 701 reports
Age 761 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with PELARGONIUM SIDOIDES?

This profile reflects 71 FDA FAERS reports that mention PELARGONIUM SIDOIDES. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PELARGONIUM SIDOIDES?

Frequently reported terms in FAERS include ASTHENIA, BLOOD PRESSURE INCREASED, DIZZINESS, DRUG DEPENDENCE, DRUG-INDUCED LIVER INJURY, HEPATOTOXICITY. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PELARGONIUM SIDOIDES?

Labeling and FAERS entries often list Schwabe North America in connection with PELARGONIUM SIDOIDES. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.