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From FDA reports: drug interactions between Famotidine, Pravastatin, Qvar 40 for a Female patient aged 68

This is a personalized study for a 68 year old female patient. The study is created by eHealthMe based on reports of 7 people who take the same drugs and have drug interactionsfrom FDA.

On Dec, 21, 2014: 7 people who reported to have interactions when taking Famotidine, Pravastatin, Qvar 40 are studied

Trend of Famotidine, Pravastatin, Qvar 40's drug interactions, side effects, and effectiveness reports (462564)

Information of the patient in this study:

Age: 68

Gender: female

Conditions: Gastritis, Hyperlipidaemia, Asthma

Drugs taking:
- Famotidine
- Pravastatin
- Qvar 40

Drug interactions have: Anaphylactic Shock, Dyspnoea, Loss Of Consciousness, Wheezing

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 68 (±5):

InteractionNumber of reports
Anaphylactic Shock (severe and rapid and sometimes fatal hypersensitivity reaction to a substance)2 (100.00%)
Dyspnoea (difficult or laboured respiration)2 (100.00%)
Loss Of Consciousness2 (100.00%)
Wheezing (a high-pitched whistling sound made while you breath)2 (100.00%)

Most common interactions experienced by females aged 68 (±5) in the use of Famotidine, Pravastatin, Qvar 40:

InteractionNumber of reports
Muscular Weakness (muscle weakness)2
Hypertension (high blood pressure)2
Hypoaesthesia (reduced sense of touch or sensation)2
Nausea (feeling of having an urge to vomit)2
Hyperlipidaemia (presence of excess lipids in the blood)2
Influenza Like Illness2
Joint Dislocation (a joint position is changed from normal position)2
Multiple Injuries2
Inguinal Hernia (hernia in which a loop of intestine enters the inguinal canal; the most common type of hernia in males)2
Hypokalaemia (low potassium)2

Most common interactions experienced by females aged 68 (±5) in long term use of Famotidine, Pravastatin, Qvar 40:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Anaphylactic Shock (severe and rapid and sometimes fatal hypersensitivity reaction to a substance)2 (28.57%)
Dyspnoea (difficult or laboured respiration)4 (57.14%)
Loss Of Consciousness2 (28.57%)
Wheezing (a high-pitched whistling sound made while you breath)2 (28.57%)

Most common interactions experienced by people in the use of Famotidine, Pravastatin, Qvar 40:

InteractionNumber of reports
Fatigue (feeling of tiredness)6
Arthralgia (joint pain)6
Condition Aggravated (worse condition)4
Dizziness4
Haemorrhage Nos4
Syncope (loss of consciousness with an inability to maintain postural tone)4
Fall4
Pain Nos4
Hypokalaemia (low potassium)4
Pulmonary Oedema Nos4

Most common interactions experienced by people in long term use of Famotidine, Pravastatin, Qvar 40:

None.

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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