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

FATIGUE ( 9 FDA reports)
TREMOR ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
FALL ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PAIN ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DEPRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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