To Know Or Not To Know About The Dangerous Actonel Drug/Procter and Gamble

To Know Or Not To Know About The Dangerous Namely Actonel Drug/Procter And Gamble
Behind Information Is Knowledge, as well as, in ones, brain. There are really people out there, who would rather know what a Pharmaceutical Drug can or may do to them, then not to have known. Remember a mind filled, with I rather not know, is a lonely sadden and afraid mind. I have to admit that at some point in life we all have had or have afraid, minds. I know I have. But through it all someone must be armed with information even if it is a family member.

Actonel Side Effects Report Physician from UNITED STATES reported ACTONEL problem on Feb 08, 2008. Female patient, 64 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: anaesthesia, bladder catheterisation, urinary retention, vaginal pain, vulvovaginitis. ACTONEL dosage: unknown. During the same period patient was treated with FEMARA. Patient recovered.

Actonel Side Effects Report
Physician from UNITED STATES reported ACTONEL problem on Feb 12, 2008. Female patient, 83 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: colostomy, diverticulitis, synovial cyst. ACTONEL dosage: 35MG ONCE A WEEK, ORAL. During the same period patient was treated with LOTREL, CALCIUM, ERGOCALCIFEROL, VITAMIN. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report
Physician from JAPAN reported ACTONEL problem on Feb 08, 2008. Female patient, 80 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: liver disorder. ACTONEL dosage: 17.5 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Feb 20, 2008. Male patient, 83 years of age, weighting 164.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, back pain, bone pain, dizziness, muscle spasms, rash, vertigo. ACTONEL dosage: unknown. Patient recovered.

Actonel Side Effects Report
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Female patient, 68 years of age, weighting 160.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: jaw disorder, nervousness, pain, tooth disorder. ACTONEL dosage: unknown. Patient recovered.

Actonel Side Effects Report
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 31, 2008. Female patient, 56 years of age, weighting 110.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abasia, activities of daily living impaired, arthralgia, arthropathy, back pain, bone pain, connective tissue disorder, dysphagia, dyspnoea. ACTONEL dosage: 35 MG WEEKLY PO. Patient recovered.

Adverse event in female receiving Actonel (Risedronate) Reported by a physician from United States on 2007-03-29 Patient: female Adverse reactions / side effects: Congenital Central Nervous System Anomaly, Skull Malformation, Drug Exposure Before Pregnancy, Abortion Induced, Cerebral Ventricle Dilatation, Antepartum Haemorrhage, Pregnancy Adverse event resulted in: death Suspect drug(s): Actonel (Risedronate)

Adverse event in 65 year old female receiving Actonel (Risedronate) Reported by a physician from United States on 2007-02-22 Patient: 65 year old female Adverse reactions / side effects: Bone Sarcoma, Neurofibroma Adverse event resulted in: death Suspect drug(s): Actonel (Risedronate)

Adverse event in female receiving Actonel (Risedronate) Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-18 Patient: female Adverse reactions / side effects: Maternal Drugs Affecting Foetus, Congenital Central Nervous System Anomaly, Skull Malformation, Drug Exposure Before Pregnancy, Abortion Induced Adverse event resulted in: death Suspect drug(s): Actonel (Risedronate)

Adverse event in 92 year old female receiving Actonel (Risedronate) Reported by a individual with unspecified qualification from France on 2007-02-22 Patient: 92 year old female, weighing 30.0 kg (66.0 pounds) Adverse reactions / side effects: Dyspepsia, Cardiac Failure, Condition Aggravated Adverse event resulted in: death Suspect drug(s): Actonel (Risedronate) Other drugs received by patient: Lasix

These Suspected Deaths and Adverse Side Effects/Events happen during the time that Procter and Gamble Owned the drug Actonel. If Doctors report deaths and nothing done, what make you think something is going to be done when people like you and I report our life threatening adverse side effects to the FDA.
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