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

ASTHENIA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
COUGH ( 4 FDA reports)
PALPITATIONS ( 3 FDA reports)
PAIN ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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