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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

RANITIDINE\RANITIDINE for Gastrooesophageal reflux disease: Side Effects & Safety Data

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There are 139 adverse event reports in the FDA FAERS database where RANITIDINE\RANITIDINE was used for Gastrooesophageal reflux disease.

Most Reported Side Effects for RANITIDINE\RANITIDINE

Side Effect Reports % Deaths Hosp.
Drug ineffective 97 13.3% 0 3
Product quality issue 56 7.7% 0 0
Pruritus 38 5.2% 0 4
Dyspnoea 32 4.4% 0 10
Insomnia 30 4.1% 0 2
Nausea 30 4.1% 0 9
Angioedema 29 4.0% 0 2
Hypotension 26 3.6% 0 21
Diarrhoea 25 3.4% 0 1
Anaphylactic reaction 24 3.3% 0 5
Malaise 24 3.3% 0 11
Abdominal pain upper 23 3.2% 0 2
Drug hypersensitivity 23 3.2% 0 4
Muscle spasms 23 3.2% 0 1
Vomiting 23 3.2% 0 11

Other Indications for RANITIDINE\RANITIDINE

Product used for unknown indication (238) Dyspepsia (74) Premedication (15) Chronic spontaneous urticaria (14) Gastritis (13) Prophylaxis against gastrointestinal ulcer (11) Prophylaxis (10) Abdominal pain upper (8) Reflux laryngitis (7) Gastric disorder (6)

Other Drugs Used for Gastrooesophageal reflux disease

RANITIDINE (141,291) OMEPRAZOLE (28,339) ESOMEPRAZOLE (27,743) PANTOPRAZOLE (18,706) LANSOPRAZOLE (17,671) DEXLANSOPRAZOLE (5,185) RABEPRAZOLE (1,689) NEXIUM (1,209) FAMOTIDINE (1,099) VONOPRAZAN (766)

Related Pages

RANITIDINE\RANITIDINE Full Profile All Gastrooesophageal reflux disease Drugs RANITIDINE\RANITIDINE Demographics RANITIDINE\RANITIDINE Timeline