SODIUM BICARBONATE, SODIUM CHLORIDE

N/A

Manufactured by CVS Pharmacy

278 FDA adverse event reports analyzed

Last updated: 2026-04-15

About SODIUM BICARBONATE, SODIUM CHLORIDE

SODIUM BICARBONATE, SODIUM CHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by CVS Pharmacy. The most commonly reported adverse reactions for SODIUM BICARBONATE, SODIUM CHLORIDE include HEADACHE, DYSPNOEA, GASTROOESOPHAGEAL REFLUX DISEASE, ASTHMA, BLOOD TEST ABNORMAL. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SODIUM BICARBONATE, SODIUM CHLORIDE.

Top Adverse Reactions

HEADACHE11 reports
DYSPNOEA10 reports
GASTROOESOPHAGEAL REFLUX DISEASE7 reports
ASTHMA6 reports
BLOOD TEST ABNORMAL6 reports
BURNING SENSATION6 reports
CARDIAC DISORDER6 reports
CARPAL TUNNEL SYNDROME6 reports
EJECTION FRACTION ABNORMAL6 reports
FIBROMYALGIA6 reports
FULL BLOOD COUNT ABNORMAL6 reports
HYPERTENSION6 reports
HYPOTHYROIDISM6 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES6 reports
OBSTRUCTIVE SLEEP APNOEA SYNDROME6 reports
POLYCYSTIC OVARIES6 reports
RENAL DISORDER6 reports
RHINITIS ALLERGIC6 reports
SENSITISATION6 reports
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION6 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE6 reports
WHEEZING6 reports
ADVERSE EVENT5 reports
HOSPITALISATION5 reports
MALAISE5 reports
NEPHRECTOMY5 reports
SLEEP APNOEA SYNDROME5 reports
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE5 reports
EJECTION FRACTION4 reports
INSOMNIA4 reports
ASTHENIA3 reports
COVID 193 reports
INCORRECT DOSE ADMINISTERED3 reports
NAUSEA3 reports
NEPHROPATHY3 reports
NIGHTMARE3 reports
OVERDOSE3 reports
ABDOMINAL DISCOMFORT2 reports
ABDOMINAL PAIN UPPER2 reports
ABNORMAL DREAMS2 reports
APPLICATION SITE ERYTHEMA2 reports
BACK PAIN2 reports
DISEASE RECURRENCE2 reports
EYE IRRITATION2 reports
EYE PAIN2 reports
FATIGUE2 reports
INCORRECT DRUG ADMINISTRATION DURATION2 reports
SLEEP DISORDER2 reports
TREATMENT NONCOMPLIANCE2 reports
VISION BLURRED2 reports
VOMITING2 reports
AGEUSIA1 reports
AGORAPHOBIA1 reports
ANAL HAEMORRHAGE1 reports
ANXIETY1 reports
APPLICATION SITE PAIN1 reports
APPLICATION SITE PRURITUS1 reports
APPLICATION SITE SWELLING1 reports
CATARACT OPERATION1 reports
CHILLS1 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE1 reports
COLD SWEAT1 reports
COMA1 reports
CONCOMITANT DISEASE AGGRAVATED1 reports
CONDITION AGGRAVATED1 reports
CONSTIPATION1 reports
COUGH1 reports
DECREASED APPETITE1 reports
DIARRHOEA1 reports
DYSPEPSIA1 reports
EUPHORIC MOOD1 reports
FALL1 reports
FEELING ABNORMAL1 reports
FUNGAL INFECTION1 reports
GAIT DISTURBANCE1 reports
GASTRIC HAEMORRHAGE1 reports
GASTROINTESTINAL DISORDER1 reports
GENERAL PHYSICAL HEALTH DETERIORATION1 reports
HAEMORRHAGE1 reports
HEPATITIS B1 reports
HUNGER1 reports
HYPERHIDROSIS1 reports
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION1 reports
INFLUENZA1 reports
INTENTIONAL PRODUCT USE ISSUE1 reports
IRRITABILITY1 reports
LOCAL SWELLING1 reports
LYME DISEASE1 reports
MANIA1 reports
MEMORY IMPAIRMENT1 reports
MOVEMENT DISORDER1 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME1 reports
MUSCULOSKELETAL DISCOMFORT1 reports
NASOPHARYNGITIS1 reports
NEUTROPENIA1 reports
OFF LABEL USE1 reports
OROPHARYNGEAL PAIN1 reports
PLEURISY1 reports
PNEUMONIA1 reports
POLYCYSTIC OVARIAN SYNDROME1 reports

Report Outcomes

Out of 34 classified reports for SODIUM BICARBONATE, SODIUM CHLORIDE:

Serious 85.3%Non-Serious 14.7%

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

Female21 (61.8%)
Male13 (38.2%)

Reports by Age

Age 547 reports
Age 573 reports
Age 723 reports
Age 372 reports
Age 211 reports
Age 441 reports
Age 481 reports
Age 491 reports
Age 511 reports
Age 521 reports
Age 601 reports
Age 631 reports
Age 641 reports
Age 651 reports
Age 661 reports
Age 681 reports
Age 731 reports
Age 761 reports
Age 771 reports
Age 891 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 SODIUM BICARBONATE, SODIUM CHLORIDE?

This profile reflects 278 FDA FAERS reports that mention SODIUM BICARBONATE, SODIUM CHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SODIUM BICARBONATE, SODIUM CHLORIDE?

Frequently reported terms in FAERS include HEADACHE, DYSPNOEA, GASTROOESOPHAGEAL REFLUX DISEASE, ASTHMA, BLOOD TEST ABNORMAL, BURNING SENSATION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures SODIUM BICARBONATE, SODIUM CHLORIDE?

Labeling and FAERS entries often list CVS Pharmacy in connection with SODIUM BICARBONATE, SODIUM CHLORIDE. 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.