LOTION

N/A

Manufactured by Derma Glove

148 FDA adverse event reports analyzed

Last updated: 2026-04-15

About LOTION

LOTION is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Derma Glove. The most commonly reported adverse reactions for LOTION include RASH, DRY SKIN, SKIN EXFOLIATION, ERYTHEMA, SKIN BURNING SENSATION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for LOTION.

Top Adverse Reactions

RASH9 reports
DRY SKIN5 reports
SKIN EXFOLIATION5 reports
ERYTHEMA4 reports
SKIN BURNING SENSATION4 reports
SWELLING FACE4 reports
DRUG INEFFECTIVE3 reports
HEADACHE3 reports
PRURITUS3 reports
RASH ERYTHEMATOUS3 reports
WEIGHT DECREASED3 reports
ACNE2 reports
ARTHRALGIA2 reports
BURNING SENSATION2 reports
CEREBROVASCULAR ACCIDENT2 reports
DYSPNOEA2 reports
HAEMORRHAGE2 reports
HYPERSENSITIVITY2 reports
MALAISE2 reports
MUSCULAR WEAKNESS2 reports
NAUSEA2 reports
OXYGEN SATURATION DECREASED2 reports
PAIN OF SKIN2 reports
PENIS DISORDER2 reports
ABDOMINAL DISCOMFORT1 reports
ABDOMINAL DISTENSION1 reports
ABDOMINAL PAIN UPPER1 reports
ABNORMAL DREAMS1 reports
ADVERSE EVENT1 reports
ANAEMIA1 reports
ANAL EROSION1 reports
ANAL HAEMORRHAGE1 reports
ANAPHYLACTIC REACTION1 reports
ANAPHYLACTIC SHOCK1 reports
ANOSMIA1 reports
ANXIETY1 reports
ARTHROPATHY1 reports
ASTHENIA1 reports
BACTERIAL INFECTION1 reports
BEDRIDDEN1 reports
BLISTER1 reports
BLOOD BLISTER1 reports
BLOOD POTASSIUM DECREASED1 reports
BLOOD PRESSURE INCREASED1 reports
C REACTIVE PROTEIN INCREASED1 reports
CARDIAC ARREST1 reports
CONFUSIONAL STATE1 reports
CONSTIPATION1 reports
COORDINATION ABNORMAL1 reports
DECREASED APPETITE1 reports
DEMENTIA1 reports
DIARRHOEA HAEMORRHAGIC1 reports
DRUG ADMINISTRATION ERROR1 reports
DYSGEUSIA1 reports
DYSKINESIA1 reports
DYSPHAGIA1 reports
DYSPHONIA1 reports
EAR DISORDER1 reports
ENERGY INCREASED1 reports
EYE DISORDER1 reports
EYE HAEMORRHAGE1 reports
EYE IRRITATION1 reports
FACIAL PAIN1 reports
FAECES PALE1 reports
FALL1 reports
FATIGUE1 reports
FEELING ABNORMAL1 reports
FEELING HOT1 reports
FOOT DEFORMITY1 reports
FURUNCLE1 reports
GAIT DISTURBANCE1 reports
GASTRIC DISORDER1 reports
GASTRIC HAEMORRHAGE1 reports
GASTROOESOPHAGEAL REFLUX DISEASE1 reports
GENITAL DISCOMFORT1 reports
GENITAL EROSION1 reports
GENITAL RASH1 reports
HALLUCINATION1 reports
HEART RATE INCREASED1 reports
HEPATIC FAILURE1 reports
HERPES ZOSTER1 reports
HOSPICE CARE1 reports
HYPOAESTHESIA1 reports
HYPOPHAGIA1 reports
IMPAIRED HEALING1 reports
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION1 reports
INSOMNIA1 reports
INTENTIONAL OVERDOSE1 reports
INTENTIONAL PRODUCT USE ISSUE1 reports
INTESTINAL HAEMORRHAGE1 reports
IRRITABILITY1 reports
KIDNEY INFECTION1 reports
LIMB DEFORMITY1 reports
LIP SWELLING1 reports
LIP ULCERATION1 reports
LISTLESS1 reports
LYME DISEASE1 reports
MALIGNANT NEOPLASM PROGRESSION1 reports
MENTAL DISORDER1 reports
MILIA1 reports

Report Outcomes

Out of 33 classified reports for LOTION:

Serious 33.3%Non-Serious 66.7%

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

Female22 (66.7%)
Male11 (33.3%)

Reports by Age

Age 582 reports
Age 732 reports
Age 772 reports
Age 121 reports
Age 181 reports
Age 191 reports
Age 291 reports
Age 331 reports
Age 351 reports
Age 361 reports
Age 381 reports
Age 491 reports
Age 511 reports
Age 521 reports
Age 541 reports
Age 621 reports
Age 641 reports
Age 651 reports
Age 661 reports
Age 701 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 LOTION?

This profile reflects 148 FDA FAERS reports that mention LOTION. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for LOTION?

Frequently reported terms in FAERS include RASH, DRY SKIN, SKIN EXFOLIATION, ERYTHEMA, SKIN BURNING SENSATION, SWELLING FACE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures LOTION?

Labeling and FAERS entries often list Derma Glove in connection with LOTION. 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.