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From FDA reports: drug interactions between Ranitidine, Hydrocodone for a Male patient aged 60

This is a personalized study for a 60 year old male patient. The study is created by eHealthMe based on reports of 542 people who take the same drugs and have drug interactionsfrom FDA.

On Oct, 26, 2014: 542 people who reported to have interactions when taking Ranitidine, Hydrocodone are studied

Trend of Ranitidine, Hydrocodone's drug interactions, side effects, and effectiveness reports (2786841)

Information of the patient in this study:

Age: 60

Gender: male

Conditions: Gastric Ulcer Haemorrhage

Drugs taking:
- Ranitidine: used for 1 - 6 months
- Hydrocodone

Drug interactions have: Blindness Unilateral, Myodesopsia, Retinal Detachment, Retinal Tear, Vitreous Haemorrhage

eHealthMe real world results:

Comparison with this patient's adverse outcomes among males aged 60 (±5):

InteractionNumber of reports
Blindness Unilateral2 (3.51%)
Myodesopsia (appearance of spots or strings in an individual's field of vision)2 (3.51%)
Retinal Detachment (a disorder of the eye in which the retina peels away from its underlying layer of support tissue)2 (3.51%)
Retinal Tear2 (3.51%)
Vitreous Haemorrhage (intraocular (inside the eye) bleeding)2 (3.51%)

Most common interactions experienced by males aged 60 (±5) in the use of Ranitidine, Hydrocodone:

InteractionNumber of reports
Anxiety46
Mitral Valve Incompetence (inefficient heart valve)36
Dyspnoea (difficult or laboured respiration)35
Anhedonia (inability to experience pleasure from activities usually found enjoyable)34
Chest Pain33
Pain30
Injury28
Bone Disorder28
Dizziness26
Spinal Corpectomy26

Most common interactions experienced by males aged 60 (±5) in long term use of Ranitidine, Hydrocodone:

None.

For people in general (regardless of gender or age):

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Blindness Unilateral2 (0.37%)
Myodesopsia (appearance of spots or strings in an individual's field of vision)2 (0.37%)
Retinal Detachment (a disorder of the eye in which the retina peels away from its underlying layer of support tissue)4 (0.74%)
Retinal Tear2 (0.37%)
Vitreous Haemorrhage (intraocular (inside the eye) bleeding)12 (2.21%)

Most common interactions experienced by people in the use of Ranitidine, Hydrocodone:

InteractionNumber of reports
Pain336
Anxiety284
Nausea (feeling of having an urge to vomit)234
Dyspnoea (difficult or laboured respiration)215
Dizziness206
Fatigue (feeling of tiredness)203
Hypertension (high blood pressure)197
Back Pain196
Vomiting185
Injury178

Most common interactions experienced by people in long term use of Ranitidine, Hydrocodone:

InteractionNumber of reports
Depression8
Anxiety8
Hepatic Failure (liver failure)6
Thrombocytopenia (decrease of platelets in blood)6
Disseminated Intravascular Coagulation (systemic activation of blood coagulation)6
Renal Failure Acute (rapid kidney dysfunction)6
Diarrhoea6
Aggression6
Psychotic Disorder6
Vomiting6

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

You can also:

NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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