LYCOPODIUM CLAVATUM SPORE

N/A

65 FDA adverse event reports analyzed

Last updated: 2026-04-15

About LYCOPODIUM CLAVATUM SPORE

LYCOPODIUM CLAVATUM SPORE is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for LYCOPODIUM CLAVATUM SPORE include DIZZINESS, DRUG INEFFECTIVE, MUSCLE SPASMS, NAUSEA, PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for LYCOPODIUM CLAVATUM SPORE.

Top Adverse Reactions

DIZZINESS3 reports
DRUG INEFFECTIVE2 reports
MUSCLE SPASMS2 reports
NAUSEA2 reports
PAIN2 reports
ABDOMINAL DISTENSION1 reports
ABDOMINAL PAIN1 reports
AGITATION1 reports
AGRAPHIA1 reports
APHASIA1 reports
ASTHENIA1 reports
BLINDNESS TRANSIENT1 reports
BLOOD PRESSURE INCREASED1 reports
CHOLESTATIC LIVER INJURY1 reports
CONSTIPATION1 reports
COUGH1 reports
DEEP VEIN THROMBOSIS1 reports
DIABETES MELLITUS INADEQUATE CONTROL1 reports
DIARRHOEA1 reports
DISTURBANCE IN ATTENTION1 reports
DYSGEUSIA1 reports
ERYTHEMA1 reports
FATIGUE1 reports
FEELING ABNORMAL1 reports
GASTRITIS1 reports
GASTROINTESTINAL HAEMORRHAGE1 reports
GENERAL PHYSICAL HEALTH DETERIORATION1 reports
HEADACHE1 reports
HEART RATE INCREASED1 reports
HOT FLUSH1 reports
HYPOAESTHESIA1 reports
INJECTION SITE ERYTHEMA1 reports
INJECTION SITE RASH1 reports
JAUNDICE CHOLESTATIC1 reports
JOINT SWELLING1 reports
LIVER DISORDER1 reports
LOCAL SWELLING1 reports
MALAISE1 reports
MENTAL IMPAIRMENT1 reports
MUSCLE STRAIN1 reports
MYOCARDIAL INFARCTION1 reports
PALPITATIONS1 reports
PANCREATIC CARCINOMA METASTATIC1 reports
PARANEOPLASTIC SYNDROME1 reports
POISONING1 reports
PORTAL HYPERTENSION1 reports
PRESYNCOPE1 reports
PRURITUS1 reports
PULMONARY ARTERIAL HYPERTENSION1 reports
PULMONARY EMBOLISM1 reports
SENSORY LOSS1 reports
SNEEZING1 reports
SOMNOLENCE1 reports
TACHYCARDIA1 reports
THROAT IRRITATION1 reports
TREATMENT FAILURE1 reports
VARICES OESOPHAGEAL1 reports
VERTIGO1 reports
WEIGHT DECREASED1 reports

Frequently Asked Questions

How many FDA adverse event reports are associated with LYCOPODIUM CLAVATUM SPORE?

This profile reflects 65 FDA FAERS reports that mention LYCOPODIUM CLAVATUM SPORE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for LYCOPODIUM CLAVATUM SPORE?

Frequently reported terms in FAERS include DIZZINESS, DRUG INEFFECTIVE, MUSCLE SPASMS, NAUSEA, PAIN, ABDOMINAL DISTENSION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

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.