Please choose an event type to view the corresponding MedsFacts report:

ASTHMA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PAIN ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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