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Ranitidine Product Quality Issue Side Effects

Ranitidine Product Quality Issue Side Effect Reports


The following Ranitidine Product Quality Issue side effect reports were submitted by healthcare professionals and consumers.

This information will help you understand how side effects, such as Product Quality Issue, can occur, and what you can do about them.

A side effect could appear soon after you start Ranitidine or it might take time to develop.



Ear Infection, Pharyngitis, Product Odour Abnormal, Product Taste Abnormal, Product Quality Issue

This Product Quality Issue side effect was reported by a consumer or non-health professional from US. A 54-year-old female patient (weight:NA) experienced the following symptoms/conditions: gastrooesophageal reflux disease. The patient was prescribed Ranitidine (dosage: NA), which was started on NS. Concurrently used drugs: NA. When starting to take Ranitidine the consumer reported the following symptoms:
  • Ear Infection
  • Pharyngitis
  • Product Odour Abnormal
  • Product Taste Abnormal
  • Product Quality Issue
These side effects may potentially be related to Ranitidine.
Product Odour Abnormal, Product Taste Abnormal, Ear Infection Bacterial, Pharyngitis, Bacterial Infection, Malaise, Nausea, Product Tampering, Product Quality Issue

This Product Quality Issue Ranitidine side effect was reported by a consumer or non-health professional from US on Mar 06, 2014. A Female , 54 years of age, weighting 182.0 lb, was diagnosed with and was treated with Ranitidine. The patient presented the following health conditions:
  • Product Odour Abnormal
  • Product Taste Abnormal
  • Ear Infection Bacterial
  • Pharyngitis
  • Bacterial Infection
  • Malaise
  • Nausea
  • Product Tampering
  • Product Quality Issue
. Ranitidine dosage: NA. Additional drugs used at the same time: NA.
Product Quality Issue

This is a Ranitidine Tablets 150 Mg Otc side effect report of a 70-year-old female patient (weight:NA) from US, suffering from the following symptoms/conditions: NA, who was treated with Ranitidine Tablets 150 Mg Otc (dosage:NA, start time: Oct 10, 2013), combined with: NA., and developed a serious reaction and a Product Quality Issue side effect. The patient presented with:
  • Product Quality Issue
which developed after the beginning of treatment. This side effect report can indicate a possible existence of increased vulnerability to Ranitidine Tablets 150 Mg Otc treatment in female patients suffering from NA, resulting in Product Quality Issue.

Urinary Tract Infection, Lethargy, Somnolence, Blood Pressure Increased, Headache, Vomiting, Product Quality Issue

A 45-year-old patient (weight: NA) from US with the following symptoms: gastrooesophageal reflux disease started Ranitidine treatment (dosage: NA) on NS. Soon after starting Ranitidine treatment, the consumer experienced several side effects, including:
  • Urinary Tract Infection
  • Lethargy
  • Somnolence
  • Blood Pressure Increased
  • Headache
  • Vomiting
  • Product Quality Issue
. Concurrently used drugs:
  • Cymbalta (duloxetine Hydrochloride)
  • Methadone (methadone)
The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Ranitidine side effects, such as Product Quality Issue.
Nausea, Vomiting, Product Odour Abnormal, Product Quality Issue

A female patient from US was prescribed and started Ranitidine on Nov 30, 2012. Patient felt the following Ranitidine side effects: nausea, vomiting, product odour abnormal, product quality issue Additional patient health information: Female , 67 years of age, The consumer reported the following symptoms: was diagnosed with and. Ranitidine dosage: 150mg Twice A Day Po. Concurrently used drugs: NA.
Anaphylactic Shock, Palpitations, Product Quality Issue, Fear

This report suggests a potential Ranitidine Hydrochloride Product Quality Issue side effect(s) that can have serious consequences. A 71-year-old female patient from PAKISTAN (weight:NA) was diagnosed with the following health condition(s): abdominal pain upper and used Ranitidine Hydrochloride (dosage: Intravenous) starting Nov 08, 2011. Soon after starting Ranitidine Hydrochloride the patient began experiencing various side effects, including:
  • Anaphylactic Shock
  • Palpitations
  • Product Quality Issue
  • Fear
Drugs used concurrently:
  • Dexamethasone
Although Ranitidine Hydrochloride demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Product Quality Issue, may still occur.
Chills, Product Quality Issue

An adverse event was reported by a physician on Aug 19, 2011 by a Female taking Ranitidine Hydrochloride (dosage: Single Dose / Intravenous) was diagnosed with and. Location: PAKISTAN , 50 years of age, weighting 143.0 lb, patient began experiencing various side effects, including: Directly after treatment started, patient experienced the unwanted or unexpected Ranitidine side effects: chills, product quality issue. Additional medications/treatments:
Associated medications used:
  • Dimenhydrinate
Product Quality Issue, Chills, Vomiting

This Product Quality Issue problem was reported by a physician from PAKISTAN. A 45-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): gastritis.On Aug 12, 2011 a consumer started treatment with Ranitidine Hydrochloride (dosage: Single Dose / Intravenous). The following drugs/medications were being taken at the same time:
  • Dimenhydrinate
When commencing Ranitidine Hydrochloride, the patient experienced the following unwanted symptoms /side effects:
  • Product Quality Issue
  • Chills
  • Vomiting
The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Product Quality Issue, may become evident only after a product is in use by the general population.
Product Quality Issue

This is a Ranitidine Hydrochloride side effect report of a 25-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: NA and was treated with Ranitidine Hydrochloride (dosage: 150 Mg, 2 In 1 D) starting Sep 27, 2011. Concurrently used drugs: NA. Soon after that, the consumer experienced the following of symptoms:
  • Product Quality Issue
This opens a possibility that Ranitidine Hydrochloride could cause Product Quality Issue and that some female patients may be more susceptible.
Laboratory Test Abnormal, Product Quality Issue, Overdose, Non-cardiac Chest Pain

This Product Quality Issue side effect was reported by a consumer or non-health professional from UNITED STATES on Oct 24, 2011. A patient from UNITED STATES , 70 years of age, weighting 196.0 lb, was treated with Ranitidine. Directly after treatment started, patient experienced the unwanted or unexpected Ranitidine side effects: laboratory test abnormal, product quality issue, overdose, non-cardiac chest pain. Ranitidine dosage: NA.
Associated medications used:
  • Lisinopril
  • Plavix
  • Plavix
  • Plavix
  • Isosorbide Dinitrate
  • Simvastatin
  • Plavix
  • Amlodipine
The patient was hospitalized. These side effects may potentially be related to Ranitidine.
Choking, Skin Discolouration, Product Quality Issue, Cough, Oropharyngeal Pain

This Product Quality Issue side effect was reported by a consumer or non-health professional from UNITED STATES. A 51-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Ranitidine (dosage: NA), which was started on Jan 01, 2010. Concurrently used drugs:
  • Trazodone
  • Cyclobenzaprine
  • Lyrica
  • Effexor
  • Advair Diskus 100/50 (1puff Twice Per Day)
  • Ventolin
  • Docusate
  • Simvastatin
When starting to take Ranitidine the consumer reported the following symptoms:
  • Choking
  • Skin Discolouration
  • Product Quality Issue
  • Cough
  • Oropharyngeal Pain
These side effects may potentially be related to Ranitidine.
Oropharyngeal Pain, Product Quality Issue, Cough, Choking, Skin Discolouration

This Product Quality Issue Ranitidine side effect was reported by a consumer or non-health professional from UNITED STATES on Mar 15, 2011. A Female , 51 years of age, was treated with Ranitidine. The patient presented the following health conditions:
  • Oropharyngeal Pain
  • Product Quality Issue
  • Cough
  • Choking
  • Skin Discolouration
. Ranitidine dosage: NA. Additional drugs used at the same time:
  • Advair Diskus 100/50 (1puff Twice Per Day)
  • Cyclobenzaprine
  • Ventolin
  • Trazodone Hcl
  • Spiriva
  • Simvastatin
  • Effexor
  • Docusate
Abdominal Discomfort, Nausea, Product Quality Issue, Product Taste Abnormal, Tooth Disorder, Unevaluable Event

This is a Ranitidine side effect report of a 48-year-old patient (weight:NA) from UNITED STATES, suffering from the following symptoms/conditions: NA, who was treated with Ranitidine (dosage:NA, start time: NS), combined with: NA., and developed a serious reaction and a Product Quality Issue side effect. The patient presented with:
  • Abdominal Discomfort
  • Nausea
  • Product Quality Issue
  • Product Taste Abnormal
  • Tooth Disorder
  • Unevaluable Event
which developed after the beginning of treatment. This side effect report can indicate a possible existence of increased vulnerability to Ranitidine treatment in patients suffering from NA, resulting in Product Quality Issue.
Finger Deformity, Hypokinesia, Malaise, Muscle Spasms, Muscle Twitching, Muscular Weakness, Product Odour Abnormal, Product Quality Issue, Tremor

A 61-year-old female patient (weight: NA) from UNITED STATES with the following symptoms: hyperchlorhydria started Ranitidine treatment (dosage: NA) on Jan 10, 2010. Soon after starting Ranitidine treatment, the consumer experienced several side effects, including:
  • Finger Deformity
  • Hypokinesia
  • Malaise
  • Muscle Spasms
  • Muscle Twitching
  • Muscular Weakness
  • Product Odour Abnormal
  • Product Quality Issue
  • Tremor
. Concurrently used drugs:
  • Citalopram Hydrobromide
  • Atenolol
  • Advair Diskus 100/50
  • Pacimol (paracetamol) Eye Drops
  • Singulair
This finding indicates that some patients can be more vulnerable to developing Ranitidine side effects, such as Product Quality Issue.
Hypokinesia, Impaired Work Ability, Malaise, Muscle Spasms, Muscle Twitching, Product Odour Abnormal, Product Quality Issue, Tremor

A female patient from UNITED STATES was prescribed and started Ranitidine Hcl on Mar 31, 2010. After Ranitidine was administered, patient encountered several Ranitidine side effects: hypokinesia, impaired work ability, malaise, muscle spasms, muscle twitching, product odour abnormal, product quality issue, tremor Additional patient health information: Female , 61 years of age, The consumer reported the following symptoms: was diagnosed with and. Ranitidine Hcl dosage: NA. Concurrently used drugs:
  • Citalopram Hydrobromide
  • Atenolol
  • Advair Diskus 100/50
  • Pacimol (paracetamol)
  • Singulair
Product Quality Issue, Product Substitution Issue

This report suggests a potential Ranitidine Product Quality Issue side effect(s) that can have serious consequences. A 57-year-old female patient from UNITED STATES (weight:NA) was diagnosed with the following health condition(s): ulcer and used Ranitidine (dosage: 1 To 2 Tablets Daily Po) starting Aug 25, 2009. Soon after starting Ranitidine the patient began experiencing various side effects, including:
  • Product Quality Issue
  • Product Substitution Issue
Drugs used concurrently:NA. Although Ranitidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Product Quality Issue, may still occur.
Erythema, Product Quality Issue, Rash, Rash Erythematous

An adverse event was reported by a consumer or non-health professional on Feb 03, 2009 by a Female taking Ranitidine (dosage: 4tsp Twice Per Day) was diagnosed with and. Location: UNITED STATES , 55 years of age, weighting 145.3 lb, patient began experiencing various side effects, including: Patient felt the following Ranitidine side effects: erythema, product quality issue, rash, rash erythematous. Additional medications/treatments:
Multiple prescriptions taken:
  • Chlor-trimeton
  • Prednisone
  • Zyrtec
  • Advair Hfa
Dyspepsia, Helicobacter Infection, Melaena, Product Quality Issue

This Product Quality Issue problem was reported by a consumer or non-health professional from SWITZERLAND. A 63-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): dyspepsia.On NS a consumer started treatment with Ranitidine Hydrochloride (dosage: 300 Mg; Qd; Po). The following drugs/medications were being taken at the same time: NA. When commencing Ranitidine Hydrochloride, the patient experienced the following unwanted symptoms /side effects:
  • Dyspepsia
  • Helicobacter Infection
  • Melaena
  • Product Quality Issue
Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Product Quality Issue, may become evident only after a product is in use by the general population.
Anorexia, Dyspepsia, Eructation, Malaise, Product Quality Issue

This is a Ranitidine side effect report of a 73-year-old female patient (weight: NA) from UNITED KINGDOM. The patient developed the following symptoms/conditions: oesophageal ulcer and was treated with Ranitidine (dosage: 150 Mg; Bid; Po) starting NS. Concurrently used drugs:
  • Bendrofluazide
  • Aspirin
  • Atorvastatin
Soon after that, the consumer experienced the following of symptoms:
  • Anorexia
  • Dyspepsia
  • Eructation
  • Malaise
  • Product Quality Issue
This opens a possibility that Ranitidine could cause Product Quality Issue and that some female patients may be more susceptible.
Product Quality Issue

This Product Quality Issue side effect was reported by a consumer or non-health professional from UNITED STATES on Feb 09, 2009. A patient from UNITED STATES , weighting 175.0 lb, was diagnosed with and was treated with Ranitidine. Patient felt the following Ranitidine side effects: product quality issue. Ranitidine dosage: 300 Mg 1 Evening. These side effects may potentially be related to Ranitidine.

DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

Ranitidine Product Quality Issue Causes and Reviews


We all need clean water. People need it to grow crops and to operate factories, and for drinking and recreation. Fish and wildlife depend on it to survive.

Many different pollutants can harm our rivers, streams, lakes, and oceans. The three most common are soil, nutrients, and bacteria. Rain washes soil into streams and rivers. The soil can kill tiny animals and fish eggs. It can clog the gills of fish and block light, causing plants to die. Nutrients, often from fertilizers, cause problems in lakes, ponds, and reservoirs. Nitrogen and phosphorus make algae grow and can turn water green. Bacteria, often from sewage spills, can pollute fresh or salt water.

You can help protect your water supply:

  • Don't pour household products such as cleansers, beauty products, medicines, auto fluids, paint, and lawn care products down the drain. Take them to a hazardous waste collection site.
  • Throw away excess household grease (meat fats, lard, cooking oil, shortening, butter, margarine, etc.) diapers, condoms, and personal hygiene products in the garbage can.
  • Clean up after your pets. Pet waste contains nutrients and germs.

Environmental Protection Agency


Ranitidine Product Quality Issue Reviews

Fri, 08 Jan 2010

Will Marinol further damage, an already diseased liver

Wed, 24 Aug 2011

Emotional Anxciety then chest pain, jaw pain on left side and headaches, I am not taking it no more. there has to be something else less tramatising to my system. It was bad enugh that i was at work when the emotional anxiety hit. not cool at all. It was like I had no control over my enotions.

Wed, 21 Sep 2011

Is Histac 150 a pain reliever for slip disc backache?

Wed, 03 Jun 2009
Has there been any evidence linking Ranitidine to lower back or hip problems?
Sat, 09 Oct 2010
<strong>gracia por la informacion</strong>
DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

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