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Ranitidine Thrombocytopenia Side Effects

Ranitidine Thrombocytopenia Side Effect Reports


The following Ranitidine Thrombocytopenia side effect reports were submitted by healthcare professionals and consumers.

This information will help you understand how side effects, such as Thrombocytopenia, 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.



Thrombocytopenia

This Thrombocytopenia side effect was reported by a pharmacist from US. A 63-year-old patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Ranitidine (dosage: NA), which was started on Jun 14, 2013. Concurrently used drugs: NA. When starting to take Ranitidine the consumer reported the following symptoms:
  • Thrombocytopenia
These side effects may potentially be related to Ranitidine.
Leukopenia, Asthenia, Thrombocytopenia, Hyperuricaemia, Pancytopenia, Anaemia

This Thrombocytopenia Ranitidine side effect was reported by a physician from HUNGARY on Apr 27, 2012. A male , weighting 218.3 lb, was treated with Ranitidine. The patient presented the following health conditions:
  • Leukopenia
  • Asthenia
  • Thrombocytopenia
  • Hyperuricaemia
  • Pancytopenia
  • Anaemia
. Ranitidine dosage: 300 Mg, 2/d. Additional drugs used at the same time:
  • Triamcinolone (Unk, 2/d)
  • Trental (1 U, 2/d)
  • Cisplatin (157 Mg, Unk)
  • Necitumumab (11f8) (ly3012211) (800 Mg, Unk)
  • Gemcitabine Hydrochloride (2625 Mg, Unk)
  • Ferrous Sulfate Tab (1 U, 2/d)
  • Amilozid (1 U, Daily (1/d))
  • Cetirizine Hcl (1 U, Daily (1/d))
The patient was hospitalized.
Histiocytosis Haematophagic, Serum Ferritin Increased, Myelodysplastic Syndrome, Thrombocytopenia, Myelocytosis

This is a Ranitidine side effect report of a 59-year-old patient (weight:NA) from FRANCE, suffering from the following symptoms/conditions: NA, who was treated with Ranitidine (dosage:NA, start time: Feb 01, 2011), combined with:
  • Dexamethasone
  • Jevtana Kit
  • Prednisone Tab
  • Taxotere
  • Corticosteroids
, and developed a serious reaction and a Thrombocytopenia side effect. The patient presented with:
  • Histiocytosis Haematophagic
  • Serum Ferritin Increased
  • Myelodysplastic Syndrome
  • Thrombocytopenia
  • Myelocytosis
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Ranitidine treatment in patients suffering from NA, resulting in Thrombocytopenia.

Thrombocytopenia, Gingival Bleeding

A 63-year-old patient (weight: NA) from ITALY with the following symptoms: prophylaxis against gastrointestinal ulcer,atrial fibrillation started Ranitidine treatment (dosage: Daily Dose 150 Mg) on Sep 15, 2010. Soon after starting Ranitidine treatment, the consumer experienced several side effects, including:
  • Thrombocytopenia
  • Gingival Bleeding
. Concurrently used drugs:
  • Aspirin (100 Mg, Qd)
This finding indicates that some patients can be more vulnerable to developing Ranitidine side effects, such as Thrombocytopenia.
Thrombocytopenia, Gingival Bleeding

A patient from ITALY was prescribed and started Ranitidine on Dec 27, 2011. Patient felt the following Ranitidine side effects: thrombocytopenia, gingival bleeding Additional patient health information: male , 63 years of age, The consumer reported the following symptoms: was diagnosed with and. Ranitidine dosage: Daily Dose 150 Mg. Concurrently used drugs:
  • Aspirin (100 Mg, Qd)
Duodenal Ulcer Perforation, Thrombocytopenia

This report suggests a potential Ranitidine Thrombocytopenia side effect(s) that can have serious consequences. A patient from CANADA (weight:NA) was diagnosed with the following health condition(s): gastrooesophageal reflux disease,constipation,cerebrovascular accident prophylaxis,gout,pain,atrial fibrillation,hyperlipidaemia,hypothyroidism,hypertension and used Ranitidine (dosage: 300 Mg) starting Oct 10, 2006. Soon after starting Ranitidine the patient began experiencing various side effects, including:
  • Duodenal Ulcer Perforation
  • Thrombocytopenia
Drugs used concurrently:
  • Lactulose
  • Dabigatran
  • Allopurinol (200 Mg)
  • Morphine Sulfate (30 Mg)
  • Dabigatran
  • Crestor (10 Mg)
  • Levothyroxine Sodium (0.1 Mg)
  • Adalat Cc (20 Mg)
The patient was hospitalized. Although Ranitidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Thrombocytopenia, may still occur.
Duodenal Ulcer Perforation, Thrombocytopenia

An adverse event was reported by a physician on Sep 27, 2011 by a male taking Ranitidine (dosage: 300 Mg) was diagnosed with and. Location: CANADA , weighting 149.9 lb, patient began experiencing various side effects, including: Directly after treatment started, patient experienced the unwanted or unexpected Ranitidine side effects: duodenal ulcer perforation, thrombocytopenia. Additional medications/treatments:
Associated medications used:
  • Carvedilol
  • Lactulose
  • Levothyroxine Sodium (0.1 Mg)
  • Dabigatran
  • Dabigatran
  • Crestor (10 Mg)
  • Carvedilol (50 Mg)
  • Morphine Sulfate (30 Mg)
The patient was hospitalized.
Thrombocytopenia, White Blood Cell Count Decreased

This Thrombocytopenia problem was reported by a health professional from INDIA. A 55-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): vomiting,pustular psoriasis.On NS a consumer started treatment with Ranitidine (dosage: 50 Mg;bid;iv). The following drugs/medications were being taken at the same time:
  • Roxithromycin (roxithromycin) (150 Mg;bid)
When commencing Ranitidine, the patient experienced the following unwanted symptoms /side effects:
  • Thrombocytopenia
  • White Blood Cell Count Decreased
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 Thrombocytopenia, may become evident only after a product is in use by the general population.
Pancytopenia, Swelling, Neutropenia, Anaemia, Thrombocytopenia, Nausea, Urogram, Transfusion Reaction, Cough

This is a Ranitidine side effect report of a female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: NA and was treated with Ranitidine (dosage: NA) starting Nov 29, 2005. Concurrently used drugs:
  • Celexa (20 Mg, Qd)
  • Aspirin
  • Multi-vitamins
  • Zometa (4 Mg, Qmo)
  • Platelets
  • Paclitaxel
  • Antihistamines
Soon after that, the consumer experienced the following of symptoms:
  • Pancytopenia
  • Swelling
  • Neutropenia
  • Anaemia
  • Thrombocytopenia
  • Nausea
  • Urogram
  • Transfusion Reaction
  • Cough
The patient was hospitalized. This opens a possibility that Ranitidine could cause Thrombocytopenia and that some female patients may be more susceptible.
Thrombocytopenia, Neutropenia

This Thrombocytopenia side effect was reported by a health professional from INDIA on Mar 07, 2011. A female patient from INDIA , 55 years of age, was treated with Ranitidine. Directly after treatment started, patient experienced the unwanted or unexpected Ranitidine side effects: thrombocytopenia, neutropenia. Ranitidine dosage: 50 Mg, Bid. The patient was hospitalized. These side effects may potentially be related to Ranitidine.
Thrombocytopenia

This Thrombocytopenia side effect was reported by a pharmacist from UNITED STATES. A 63-year-old patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Ranitidine (dosage: NA), which was started on Mar 23, 2010. Concurrently used drugs: NA. When starting to take Ranitidine the consumer reported the following symptoms:
  • Thrombocytopenia
The patient was hospitalized. These side effects may potentially be related to Ranitidine.
Contusion, Thrombocytopenia

This Thrombocytopenia Ranitidine Hydrochloride 16028/0122 83.75 Mg side effect was reported by a health professional from UNITED KINGDOM on Jan 05, 2010. A male , 45 years of age, was treated with Ranitidine Hydrochloride 16028/0122 83.75 Mg. The patient presented the following health conditions:
  • Contusion
  • Thrombocytopenia
. Ranitidine Hydrochloride 16028/0122 83.75 Mg dosage: Unk. Additional drugs used at the same time:
  • Darunavir (800 Mg, Qd)
  • Omeprazole (Unk)
  • Ritonavir (100 Mg, Qd)
Thrombocytopenia

This is a Ranitidine side effect report of a 72-year-old patient (weight:NA) from UNITED STATES, suffering from the following symptoms/conditions: gastrointestinal disorder,prophylaxis, who was treated with Ranitidine (dosage:50 Mg Tid Iv, start time: Apr 14, 2008), combined with: NA., and developed a serious reaction and a Thrombocytopenia side effect. The patient presented with:
  • Thrombocytopenia
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Ranitidine treatment in patients suffering from gastrointestinal disorder,prophylaxis, resulting in Thrombocytopenia.
Hypoxia, Lower Respiratory Tract Infection, Overdose, Pyrexia, Renal Failure Acute, Tachycardia, Thrombocytopenia

A 27-year-old patient (weight: NA) from UNITED KINGDOM with the following symptoms: NA started Ranitidine treatment (dosage: 150 Mg;bid;po) on NS. Soon after starting Ranitidine treatment, the consumer experienced several side effects, including:
  • Hypoxia
  • Lower Respiratory Tract Infection
  • Overdose
  • Pyrexia
  • Renal Failure Acute
  • Tachycardia
  • Thrombocytopenia
. Concurrently used drugs:
  • Clozaril
  • Hyoscine Hbr Hyt
  • Valproic Acid
  • Cocaine
The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Ranitidine side effects, such as Thrombocytopenia.
Blood Creatine Phosphokinase Increased, Hypoxia, Lower Respiratory Tract Infection, Overdose, Pyrexia, Renal Failure Acute, Tachycardia, Thrombocytopenia

A patient from UNITED KINGDOM was prescribed and started Ranitidine on Jan 14, 2008. After Ranitidine was administered, patient encountered several Ranitidine side effects: blood creatine phosphokinase increased, hypoxia, lower respiratory tract infection, overdose, pyrexia, renal failure acute, tachycardia, thrombocytopenia Additional patient health information: male , 27 years of age, The consumer reported the following symptoms: . Ranitidine dosage: 150 Mg; Twice A Day, 1050 Mg; Daily. Concurrently used drugs:
  • Hyoscine Hbr Hyt (210 Mg;, 300 Ug;)
  • Clozaril (6100 Mg;, 450 Mg; Daily)
  • Clozaril (6100 Mg;, 450 Mg; Daily)
  • Clozaril (6100 Mg;, 450 Mg; Daily)
  • Cocaine (cocaine)
  • Valproate Sodium (9600 Mg; Daily, 800 Mg; Twice A Day)
The patient was hospitalized.
Blood Creatine Phosphokinase Increased, C-reactive Protein Increased, Hypoxia, Lower Respiratory Tract Infection, Overdose, Pyrexia, Renal Failure Acute, Tachycardia, Thrombocytopenia

This report suggests a potential Ranitidine Thrombocytopenia side effect(s) that can have serious consequences. A 27-year-old patient from UNITED KINGDOM (weight:NA) was diagnosed with the following health condition(s): NA and used Ranitidine (dosage: 150 Mg; Twice A Day; 1050 Mg;daily) starting Jun 04, 2007. Soon after starting Ranitidine the patient began experiencing various side effects, including:
  • Blood Creatine Phosphokinase Increased
  • C-reactive Protein Increased
  • Hypoxia
  • Lower Respiratory Tract Infection
  • Overdose
  • Pyrexia
  • Renal Failure Acute
  • Tachycardia
  • Thrombocytopenia
Drugs used concurrently:
  • Hyoscine Hbr Hyt (210 Mg; 300 Ug)
  • Clozaril (6100 Mg; 450 Mg; Daily)
  • Clozaril (6100 Mg; 450 Mg; Daily)
  • Cocaine (cocaine)
  • Valproate Sodium (9600 Mg;daily; 800 Mg; Twice A Day)
The patient was hospitalized. Although Ranitidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Thrombocytopenia, may still occur.
Blood Creatine Phosphokinase Increased, C-reactive Protein Increased, Hypoxia, Lower Respiratory Tract Infection, Overdose, Pyrexia, Renal Failure Acute, Tachycardia, Thrombocytopenia

An adverse event was reported by a consumer or non-health professional on Jan 11, 2008 by a male taking Ranitidine (dosage: 300mg Per Day) . Location: UNITED KINGDOM , 27 years of age, patient began experiencing various side effects, including: Patient felt the following Ranitidine side effects: blood creatine phosphokinase increased, c-reactive protein increased, hypoxia, lower respiratory tract infection, overdose, pyrexia, renal failure acute, tachycardia, thrombocytopenia. Additional medications/treatments: The patient was hospitalized.
Thrombocytopenia

This Thrombocytopenia problem was reported by a pharmacist from UNITED STATES. A 71-year-old patient (weight: NA) was diagnosed with the following medical condition(s): NA.On NS a consumer started treatment with Ranitidine (dosage: NA). The following drugs/medications were being taken at the same time:
  • Hydrochlorothiazide
When commencing Ranitidine, the patient experienced the following unwanted symptoms /side effects:
  • Thrombocytopenia
Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as Thrombocytopenia, may become evident only after a product is in use by the general population.
Thrombocytopenia

This is a Ranitidine side effect report of a patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: NA and was treated with Ranitidine (dosage: 50 Mg Q 8 Hrs Iv) starting Jan 07, 2006. Concurrently used drugs: NA. Soon after that, the consumer experienced the following of symptoms:
  • Thrombocytopenia
This opens a possibility that Ranitidine could cause Thrombocytopenia and that some patients may be more susceptible.
Thrombocytopenia

This Thrombocytopenia side effect was reported by a consumer or non-health professional from on Jan 26, 2005. A female patient from , 74 years of age, weighting 132.3 lb, was diagnosed with and was treated with Ranitidine. Patient felt the following Ranitidine side effects: thrombocytopenia. Ranitidine dosage: 50mg Twice Per Day.
Multiple prescriptions taken:
  • Drotrecogin Alfa-recombinant Human Activated Protein C (120mg Per Day)
  • Cefuroxime (750mg Three Times Per Day)
  • Metronidazole (500mg Three Times Per Day)
  • Amoxicillin (2g Three Times Per Day)
  • Benzylpenicillin
  • Heparin
These side effects may potentially be related to Ranitidine.

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

Ranitidine Thrombocytopenia Causes and Reviews


Platelets are little pieces of blood cells. Platelets help wounds heal and prevent bleeding by forming blood clots. Your bone marrow makes platelets. Problems can result from having too few or too many platelets, or from platelets that do not work properly.

If your blood has a low number of platelets, it is called Thrombocytopenia. This can put you at risk for mild to serious bleeding. If your blood has too many platelets, you may have a higher risk of blood clots. With other platelet disorders, the platelets do not work as they should. For example, in von Willebrand Disease, the platelets cannot stick together or cannot attach to blood vessel walls. This can cause excessive bleeding.

Treatment of platelet disorders depends on the cause.

NIH: National Heart, Lung, and Blood Institute


Ranitidine Thrombocytopenia 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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