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From FDA reports: drug interactions between Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg for a Female patient aged 71

This is a personalized study for a 71 year old female patient. The study is created by eHealthMe based on reports of 210 people who take the same drugs and have drug interactionsfrom FDA.

On Oct, 26, 2014: 210 people who reported to have interactions when taking Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg are studied

Trend of Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg's drug interactions, side effects, and effectiveness reports (2793948)

Information of the patient in this study:

Age: 71

Gender: female

Conditions: Osteoporosis

Drugs taking:
- Alendronate Sodium Tablets Usp 70 Mg: used for 1 - 6 months
- Alendronate Sodium Tablets Usp 70mg

Drug interactions have: Abdominal Distension, Abdominal Pain Upper, Arthralgia, Dry Mouth, Dyspepsia, Flatulence, Headache, Pain In Extremity, Product Quality Issue

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 71 (±5):

InteractionNumber of reports
Abdominal Distension2 (4.26%)
Abdominal Pain Upper4 (8.51%)
Arthralgia (joint pain)2 (4.26%)
Dry Mouth2 (4.26%)
Dyspepsia (indigestion)8 (17.02%)
Flatulence (flatus expelled through the anus)10 (21.28%)
Headache (pain in head)5 (10.64%)
Pain In Extremity6 (12.77%)
Product Quality Issue2 (4.26%)

Most common interactions experienced by females aged 71 (±5) in the use of Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg:

InteractionNumber of reports
Fall10
Flatulence (flatus expelled through the anus)10
Dyspepsia (indigestion)8
Pruritus (severe itching of the skin)8
Asthenia (weakness)8
Cough8
Dyspnoea (difficult or laboured respiration)8
Dermatitis Nos7
Constipation6
Anxiety6

Most common interactions experienced by females aged 71 (±5) in long term use of Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg:

InteractionNumber of reports
Osteomyelitis (infection of bone)2
Osteonecrosis (death of bone)2
Thrombocytopenia (decrease of platelets in blood)2
Vision Blurred2
Headache (pain in head)2
Hand Fracture2
Laceration (tearing of soft body tissue)2
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)2
Hypersensitivity2
International Normalised Ratio Increased2

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Abdominal Distension8 (3.81%)
Abdominal Pain Upper12 (5.71%)
Arthralgia (joint pain)32 (15.24%)
Dry Mouth24 (11.43%)
Dyspepsia (indigestion)12 (5.71%)
Flatulence (flatus expelled through the anus)16 (7.62%)
Headache (pain in head)42 (20.00%)
Pain In Extremity22 (10.48%)
Product Quality Issue2 (0.95%)

Most common interactions experienced by people in the use of Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg:

InteractionNumber of reports
Hypertension (high blood pressure)43
Headache (pain in head)42
Fall42
Nausea (feeling of having an urge to vomit)42
Fatigue (feeling of tiredness)38
Anxiety36
Depression34
Pneumonia33
Arthralgia (joint pain)32
Drug Hypersensitivity32

Most common interactions experienced by people in long term use of Alendronate Sodium Tablets Usp 70 Mg, Alendronate Sodium Tablets Usp 70mg:

InteractionNumber of reports
Hypertension (high blood pressure)23
Headache (pain in head)23
Depression23
Drug Hypersensitivity23
Osteomyelitis (infection of bone)22
Osteonecrosis (death of bone)22
Overdose20
Adverse Drug Reaction20
Sinusitis (inflammation of sinus)20
Myositis (inflammation of the muscles)18

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.

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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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