AMMONIUM LACTATE

N/A

Manufactured by Padagis Israel Pharmaceuticals Ltd

4,560 FDA adverse event reports analyzed

Last updated: 2026-04-15

About AMMONIUM LACTATE

AMMONIUM LACTATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Padagis Israel Pharmaceuticals Ltd. The most commonly reported adverse reactions for AMMONIUM LACTATE include PAIN, FATIGUE, CHRONIC KIDNEY DISEASE, DIARRHOEA, DRUG INEFFECTIVE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for AMMONIUM LACTATE.

Top Adverse Reactions

PAIN138 reports
FATIGUE137 reports
CHRONIC KIDNEY DISEASE127 reports
DIARRHOEA127 reports
DRUG INEFFECTIVE120 reports
NAUSEA114 reports
RASH102 reports
DYSPNOEA101 reports
RENAL FAILURE99 reports
FALL95 reports
HEADACHE93 reports
ANXIETY91 reports
ACUTE KIDNEY INJURY90 reports
DEATH86 reports
DIZZINESS77 reports
OFF LABEL USE77 reports
PRURITUS77 reports
ARTHRALGIA72 reports
VOMITING68 reports
PAIN IN EXTREMITY66 reports
EMOTIONAL DISTRESS63 reports
WEIGHT DECREASED61 reports
PRODUCT DOSE OMISSION ISSUE60 reports
CONSTIPATION59 reports
ASTHENIA58 reports
BACK PAIN58 reports
PNEUMONIA55 reports
DEPRESSION54 reports
END STAGE RENAL DISEASE54 reports
DRY SKIN53 reports
ANHEDONIA52 reports
GAIT DISTURBANCE49 reports
MALAISE48 reports
HYPERTENSION47 reports
COUGH45 reports
DECREASED APPETITE44 reports
PRODUCT USE IN UNAPPROVED INDICATION43 reports
CONDITION AGGRAVATED42 reports
INSOMNIA42 reports
COVID 1939 reports
CHEST PAIN38 reports
TREMOR38 reports
ECONOMIC PROBLEM37 reports
SOMNOLENCE37 reports
URINARY TRACT INFECTION37 reports
DERMATITIS ATOPIC36 reports
ANAEMIA35 reports
FEELING ABNORMAL35 reports
MUSCLE SPASMS33 reports
GASTROOESOPHAGEAL REFLUX DISEASE32 reports
INJECTION SITE PAIN32 reports
PSORIASIS32 reports
HYPOAESTHESIA31 reports
HYPOTENSION31 reports
VISION BLURRED31 reports
CONFUSIONAL STATE30 reports
MYALGIA30 reports
PYREXIA29 reports
ERYTHEMA28 reports
OSTEOPOROSIS28 reports
PERIPHERAL SWELLING28 reports
BLOOD PRESSURE INCREASED27 reports
MEMORY IMPAIRMENT27 reports
SKIN EXFOLIATION27 reports
ABDOMINAL PAIN UPPER26 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION26 reports
ALOPECIA25 reports
BONE DENSITY DECREASED25 reports
EYE PAIN25 reports
HOSPITALISATION25 reports
ILLNESS25 reports
NEUROPATHY PERIPHERAL25 reports
ABDOMINAL PAIN24 reports
ASTHMA24 reports
BLOOD GLUCOSE INCREASED24 reports
CARDIAC FAILURE CONGESTIVE24 reports
CELLULITIS24 reports
CEREBROVASCULAR ACCIDENT24 reports
NEPHROGENIC ANAEMIA24 reports
WEIGHT INCREASED24 reports
ABDOMINAL DISCOMFORT23 reports
CONTUSION23 reports
DEEP VEIN THROMBOSIS23 reports
INFECTION23 reports
SEPSIS23 reports
SLEEP DISORDER23 reports
BALANCE DISORDER22 reports
INTENTIONAL PRODUCT USE ISSUE21 reports
OROPHARYNGEAL PAIN21 reports
ATRIAL FIBRILLATION20 reports
VISUAL IMPAIRMENT20 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS20 reports
BRONCHITIS19 reports
DEHYDRATION19 reports
DRUG HYPERSENSITIVITY19 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES19 reports
MUSCULAR WEAKNESS19 reports
OEDEMA PERIPHERAL19 reports
PRODUCT DOSE OMISSION IN ERROR19 reports
PRODUCT USE ISSUE19 reports

Report Outcomes

Out of 1,934 classified reports for AMMONIUM LACTATE:

Serious 56.5%Non-Serious 43.5%

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

Female1,036 (58.4%)
Male737 (41.5%)
Unknown2 (0.1%)

Reports by Age

Age 6544 reports
Age 6342 reports
Age 7242 reports
Age 6738 reports
Age 6637 reports
Age 6035 reports
Age 6835 reports
Age 7035 reports
Age 6132 reports
Age 6231 reports
Age 7430 reports
Age 6929 reports
Age 7529 reports
Age 5928 reports
Age 7627 reports
Age 6425 reports
Age 8225 reports
Age 5724 reports
Age 7124 reports
Age 8024 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 AMMONIUM LACTATE?

This profile reflects 4,560 FDA FAERS reports that mention AMMONIUM LACTATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for AMMONIUM LACTATE?

Frequently reported terms in FAERS include PAIN, FATIGUE, CHRONIC KIDNEY DISEASE, DIARRHOEA, DRUG INEFFECTIVE, NAUSEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures AMMONIUM LACTATE?

Labeling and FAERS entries often list Padagis Israel Pharmaceuticals Ltd in connection with AMMONIUM LACTATE. 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.